Quality Asia Peeragarhi, Delhi

  • ISO 24442 Certification Service

    ISO 24442 Certification Service

    25,000 / Set

    • Type of CertificationISO 24442
    • Industry FocusDiverse
    • Certification Body AccreditationNABCB
    • Implementation Timeline20 days
    • CostBased On Company Size & Complexity
    • ISO 24442:2011 Certification – Quality Asia Certification Overview ISO 24442:2011 specifies a standardized method for determining the sun protection factor (SPF) of sunscreen products using in vivo testing on human skin. The SPF value represents the level of protection a product offers against UVB radiation, the main cause of sunburn and skin damage. This standard helps ensure consistency, accuracy, and comparability in SPF measurements across the globe, offering consumers reliable information on product effectiveness. What is ISO 24442:2011? ISO 24442:2011 is an internationally recognized standard that defines in vivo procedures for evaluating the sun protection factor (SPF) of sunscreen products applied to the skin. It outlines the testing methodology, including subject selection, application amount, UV exposure, and data analysis. The test results obtained are essential for labeling and regulatory purposes, helping manufacturers demonstrate the claimed SPF values of their products with scientifically backed results. This standard is widely accepted in global markets and ensures that sunscreen products meet safety and efficacy requirements. Why ISO 24442:2011 Certification? Achieving ISO 24442:2011 certification demonstrates a product 's compliance with validated international testing methods for SPF measurement. It helps manufacturers, laboratories, and distributors ensure product claims are truthful and based on robust testing. This certification is particularly important for organizations operating in regulated markets or aiming for consumer trust through transparency and reliability. It also supports alignment with regulatory bodies, such as the FDA, European Commission, and other national health authorities. Benefits of ISO 24442:2011 Certification Product Credibility: Validates SPF claims through standardized in vivo testing, ensuring credibility and consistency across batches. Market Access: Facilitates entry into international markets by meeting globally accepted SPF testing requirements. Customer Trust: Enhances consumer confidence in the product 's sun protection efficacy and safety. Regulatory Compliance: Supports adherence to national and international guidelines for cosmetic and skincare product labeling. Competitive Edge: Distinguishes products in a crowded market through scientifically validated performance indicators. Risk Reduction: Minimizes legal and reputational risks associated with inaccurate or exaggerated SPF claims. ISO 24442:2011 Certification Process Application & Review: Submission of product details, intended SPF claim, and testing requirements. Testing Procedure: Conduct of in vivo testing in accordance with ISO 24442 guidelines, including subject recruitment, product application, and controlled UV exposure. Data Evaluation: Analysis of UV-induced erythema and statistical validation of SPF results. Documentation Audit: Verification of test reports, protocols, and quality management documents. Issuance of Certificate: Granting of certification upon successful verification of compliance with the standard. Required Documents Before Audit   Product specification sheet and formulation details Test protocol aligned with ISO 24442 methodology Ethical clearance for in vivo testing (if required by local laws) Volunteer consent forms and test site documentation Quality control and assurance records Previous SPF test reports (if applicable) Calibration records of UV source and measurement instruments
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  • ISO 24442 Certification Service

    ISO 24442 Certification Service

    25,000 / Set

    ISO 24442:2011 Certification – Quality Asia Certification Overview ISO 24442:2011 specifies a standardized method for determining the sun protection factor (SPF) of sunscreen products using in vivo testing on human skin. The SPF value represents the level of protection a product offers against UVB radiation, the main cause of sunburn and skin damage. This standard helps ensure consistency, accuracy, and comparability in SPF measurements across the globe, offering consumers reliable information on product effectiveness. What is ISO 24442:2011? ISO 24442:2011 is an internationally recognized standard that defines in vivo procedures for evaluating the sun protection factor (SPF) of sunscreen products applied to the skin. It outlines the testing methodology, including subject selection, application amount, UV exposure, and data analysis. The test results obtained are essential for labeling and regulatory purposes, helping manufacturers demonstrate the claimed SPF values of their products with scientifically backed results. This standard is widely accepted in global markets and ensures that sunscreen products meet safety and efficacy requirements. Why ISO 24442:2011 Certification? Achieving ISO 24442:2011 certification demonstrates a product 's compliance with validated international testing methods for SPF measurement. It helps manufacturers, laboratories, and distributors ensure product claims are truthful and based on robust testing. This certification is particularly important for organizations operating in regulated markets or aiming for consumer trust through transparency and reliability. It also supports alignment with regulatory bodies, such as the FDA, European Commission, and other national health authorities. Benefits of ISO 24442:2011 Certification Product Credibility: Validates SPF claims through standardized in vivo testing, ensuring credibility and consistency across batches. Market Access: Facilitates entry into international markets by meeting globally accepted SPF testing requirements. Customer Trust: Enhances consumer confidence in the product 's sun protection efficacy and safety. Regulatory Compliance: Supports adherence to national and international guidelines for cosmetic and skincare product labeling. Competitive Edge: Distinguishes products in a crowded market through scientifically validated performance indicators. Risk Reduction: Minimizes legal and reputational risks associated with inaccurate or exaggerated SPF claims. ISO 24442:2011 Certification Process Application & Review: Submission of product details, intended SPF claim, and testing requirements. Testing Procedure: Conduct of in vivo testing in accordance with ISO 24442 guidelines, including subject recruitment, product application, and controlled UV exposure. Data Evaluation: Analysis of UV-induced erythema and statistical validation of SPF results. Documentation Audit: Verification of test reports, protocols, and quality management documents. Issuance of Certificate: Granting of certification upon successful verification of compliance with the standard. Required Documents Before Audit   Product specification sheet and formulation details Test protocol aligned with ISO 24442 methodology Ethical clearance for in vivo testing (if required by local laws) Volunteer consent forms and test site documentation Quality control and assurance records Previous SPF test reports (if applicable) Calibration records of UV source and measurement instruments

    Type of Certification : ISO 24442

    Industry Focus : Diverse

    Certification Body Accreditation : NABCB

    Implementation Timeline : 20 days

    Cost : Based On Company Size & Complexity

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  • ISO 20488 Certificate Service

    ISO 20488 Certificate Service

    25,000 / Set

    • Type of CertificationISO 20488
    • Industry FocusDiverse
    • Certification Body AccreditationNABCB
    • Implementation Timeline20 days
    • CostBased On Company Size & Complexity
    • What is ISO 20488:2018? ISO 20488:2018 is an international standard that provides guidelines for online consumer review principles and practices. It ensures the collection, moderation, and publication of consumer reviews are carried out transparently, fairly, and without manipulation. This standard helps organizations build consumer trust and protect the integrity of digital reviews on websites, apps, and platforms. By following ISO 20488, businesses demonstrate accountability, credibility, and commitment to unbiased customer feedback. ISO 20488 – Overview ISO 20488:2018 is designed to improve the reliability of online consumer reviews. In today’s digital age, customer reviews play a crucial role in influencing purchase decisions. The standard establishes best practices for how reviews are collected, verified, and displayed, ensuring both consumers and businesses are treated fairly. It applies to all types of online review systems, including e-commerce platforms, service websites, booking apps, and feedback tools. The goal is to reduce fake reviews, ensure honest user experiences, and protect consumers from misleading information. ISO 20488:2018 Key Requirements Implement clear policies for review submission and verification. Ensure reviewers are genuine customers or users of the product or service. Avoid any manipulation, deletion, or artificial promotion of reviews. Provide equal opportunity for negative and positive feedback. Maintain transparency in review moderation and response processes. Disclose any sponsorship or incentivization related to submitted reviews. Enable users to report suspicious or abusive reviews easily. Protect personal data shared during the review process. ISO 20488 Training and Implementation Support Quality Asia Certification supports organizations in implementing ISO 20488:2018 by ensuring their online review systems follow ethical and transparent standards. We help organizations adopt policies and review processes that are aligned with the standard’s core principles—integrity, transparency, privacy, and impartiality. Our approach promotes responsible online behavior and builds consumer confidence in digital review platforms. ISO 20488 Certification Preparation Process Review System Assessment – Evaluate current mechanisms for collecting and managing consumer reviews. Policy Alignment – Ensure internal policies meet ISO 20488 standards for fairness, accuracy, and moderation. Implementation – Establish controls to validate reviewer identity and prevent review fraud. Audit Readiness – Perform checks to ensure the review platform aligns with all ISO 20488:2018 clauses. Continuous Monitoring – Maintain system integrity through ongoing oversight and review handling procedures.   Contact Us for ISO 20488 Certification If your organization hosts or manages online reviews and aims to strengthen the authenticity and transparency of user feedback, ISO 20488:2018 is the ideal standard. Quality Asia Certification offers end-to-end certification services to help you validate your review management system. Achieve global recognition for ethical digital practices and foster stronger trust with your customers through ISO 20488 certification. Let us help you demonstrate your commitment to fair and trustworthy online engagement.
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  • ISO 20488 Certificate Service

    ISO 20488 Certificate Service

    25,000 / Set

    What is ISO 20488:2018? ISO 20488:2018 is an international standard that provides guidelines for online consumer review principles and practices. It ensures the collection, moderation, and publication of consumer reviews are carried out transparently, fairly, and without manipulation. This standard helps organizations build consumer trust and protect the integrity of digital reviews on websites, apps, and platforms. By following ISO 20488, businesses demonstrate accountability, credibility, and commitment to unbiased customer feedback. ISO 20488 – Overview ISO 20488:2018 is designed to improve the reliability of online consumer reviews. In today’s digital age, customer reviews play a crucial role in influencing purchase decisions. The standard establishes best practices for how reviews are collected, verified, and displayed, ensuring both consumers and businesses are treated fairly. It applies to all types of online review systems, including e-commerce platforms, service websites, booking apps, and feedback tools. The goal is to reduce fake reviews, ensure honest user experiences, and protect consumers from misleading information. ISO 20488:2018 Key Requirements Implement clear policies for review submission and verification. Ensure reviewers are genuine customers or users of the product or service. Avoid any manipulation, deletion, or artificial promotion of reviews. Provide equal opportunity for negative and positive feedback. Maintain transparency in review moderation and response processes. Disclose any sponsorship or incentivization related to submitted reviews. Enable users to report suspicious or abusive reviews easily. Protect personal data shared during the review process. ISO 20488 Training and Implementation Support Quality Asia Certification supports organizations in implementing ISO 20488:2018 by ensuring their online review systems follow ethical and transparent standards. We help organizations adopt policies and review processes that are aligned with the standard’s core principles—integrity, transparency, privacy, and impartiality. Our approach promotes responsible online behavior and builds consumer confidence in digital review platforms. ISO 20488 Certification Preparation Process Review System Assessment – Evaluate current mechanisms for collecting and managing consumer reviews. Policy Alignment – Ensure internal policies meet ISO 20488 standards for fairness, accuracy, and moderation. Implementation – Establish controls to validate reviewer identity and prevent review fraud. Audit Readiness – Perform checks to ensure the review platform aligns with all ISO 20488:2018 clauses. Continuous Monitoring – Maintain system integrity through ongoing oversight and review handling procedures.   Contact Us for ISO 20488 Certification If your organization hosts or manages online reviews and aims to strengthen the authenticity and transparency of user feedback, ISO 20488:2018 is the ideal standard. Quality Asia Certification offers end-to-end certification services to help you validate your review management system. Achieve global recognition for ethical digital practices and foster stronger trust with your customers through ISO 20488 certification. Let us help you demonstrate your commitment to fair and trustworthy online engagement.

    Type of Certification : ISO 20488

    Industry Focus : Diverse

    Certification Body Accreditation : NABCB

    Implementation Timeline : 20 days

    Cost : Based On Company Size & Complexity

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Services
  • SOX Compliance

    SOX Compliance

    25,000 / Number

    • TypeSOX
    • What is SOX (Sarbanes–Oxley Act of 2002)? SOX, or the Sarbanes–Oxley Act of 2002, is a United States federal law that sets enhanced standards for all U.S. public company boards, management, and public accounting firms. It was enacted to restore investor confidence after major corporate scandals and mandates strict reforms to improve financial disclosures, prevent accounting fraud, and enforce internal control mechanisms. While primarily applicable to U.S.-listed companies, it has also impacted global firms with U.S. operations or partnerships. SOX – Overview SOX focuses on protecting shareholders and the general public from accounting errors and fraudulent practices in enterprises. It emphasizes the importance of transparency in financial reporting and accountability in corporate governance. The Act includes provisions that directly impact internal audits, risk management processes, IT security controls, and executive-level responsibilities. Sections 302 and 404 are among the most critical parts, requiring executive certification of financial reports and assessment of internal control effectiveness. SOX Compliance Key Requirements Establish internal controls over financial reporting and disclose their effectiveness. Ensure CEO and CFO personally certify the accuracy of financial statements. Maintain secure and tamper-proof record-keeping for a defined retention period. Enable traceability and accountability for data changes and user actions. Implement IT security controls to protect financial data and systems. Provide regular testing and documentation of controls related to financial operations. Ensure timely disclosures of material changes in financial condition. Set up whistleblower policies and anonymous reporting mechanisms. SOX Internal Control Implementation and Auditing Organizations subject to SOX must maintain a strong system of internal control over financial reporting (ICFR). This includes well-defined documentation of procedures, risk assessments, and evidence of control testing. Regular audits are conducted to verify the effectiveness of these controls. Key areas covered include general IT controls, user access management, system change monitoring, and segregation of duties. Financial systems and ERPs are configured to comply with SOX requirements, with a focus on data integrity and traceability. SOX Certification Support Process Readiness Review – Evaluate internal systems and controls for compliance scope. Documentation – Maintain formal records of controls, testing logs, and risk mappings. Implementation Review – Ensure appropriate IT and financial safeguards are in place. Audit Facilitation – Support structured internal and external audits for SOX validation. Ongoing Monitoring – Regularly assess and update internal control measures to align with compliance goals.   Contact Us for SOX Certification Services Quality Asia Certification offers end-to-end support for SOX certification. Whether your organization is required to comply due to listing obligations or voluntary alignment with financial governance best practices, our team ensures systematic assessment and readiness. We focus on providing structured auditing, control verification, and certification aligned with SOX provisions. Ensure your organization upholds transparency, accountability, and investor trust by aligning with the Sarbanes–Oxley Act of 2002.
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  • SOX Compliance

    SOX Compliance

    25,000 / Number

    What is SOX (Sarbanes–Oxley Act of 2002)? SOX, or the Sarbanes–Oxley Act of 2002, is a United States federal law that sets enhanced standards for all U.S. public company boards, management, and public accounting firms. It was enacted to restore investor confidence after major corporate scandals and mandates strict reforms to improve financial disclosures, prevent accounting fraud, and enforce internal control mechanisms. While primarily applicable to U.S.-listed companies, it has also impacted global firms with U.S. operations or partnerships. SOX – Overview SOX focuses on protecting shareholders and the general public from accounting errors and fraudulent practices in enterprises. It emphasizes the importance of transparency in financial reporting and accountability in corporate governance. The Act includes provisions that directly impact internal audits, risk management processes, IT security controls, and executive-level responsibilities. Sections 302 and 404 are among the most critical parts, requiring executive certification of financial reports and assessment of internal control effectiveness. SOX Compliance Key Requirements Establish internal controls over financial reporting and disclose their effectiveness. Ensure CEO and CFO personally certify the accuracy of financial statements. Maintain secure and tamper-proof record-keeping for a defined retention period. Enable traceability and accountability for data changes and user actions. Implement IT security controls to protect financial data and systems. Provide regular testing and documentation of controls related to financial operations. Ensure timely disclosures of material changes in financial condition. Set up whistleblower policies and anonymous reporting mechanisms. SOX Internal Control Implementation and Auditing Organizations subject to SOX must maintain a strong system of internal control over financial reporting (ICFR). This includes well-defined documentation of procedures, risk assessments, and evidence of control testing. Regular audits are conducted to verify the effectiveness of these controls. Key areas covered include general IT controls, user access management, system change monitoring, and segregation of duties. Financial systems and ERPs are configured to comply with SOX requirements, with a focus on data integrity and traceability. SOX Certification Support Process Readiness Review – Evaluate internal systems and controls for compliance scope. Documentation – Maintain formal records of controls, testing logs, and risk mappings. Implementation Review – Ensure appropriate IT and financial safeguards are in place. Audit Facilitation – Support structured internal and external audits for SOX validation. Ongoing Monitoring – Regularly assess and update internal control measures to align with compliance goals.   Contact Us for SOX Certification Services Quality Asia Certification offers end-to-end support for SOX certification. Whether your organization is required to comply due to listing obligations or voluntary alignment with financial governance best practices, our team ensures systematic assessment and readiness. We focus on providing structured auditing, control verification, and certification aligned with SOX provisions. Ensure your organization upholds transparency, accountability, and investor trust by aligning with the Sarbanes–Oxley Act of 2002.

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  • soc 3 certification consultancy

    soc 3 certification consultancy

    25,000 / Set

    • Brand NameSOC-3 Type 1,2 Report
    • What is SOC 3 Type 1 & Type 2? SOC 3 (System and Organization Controls 3) reports are designed to assure the public about the integrity and security of a service organization 's systems. Based on the AICPA Trust Services Criteria, SOC 3 evaluates controls related to Security, Availability, Processing Integrity, Confidentiality, and Privacy. Unlike SOC 2, SOC 3 reports are general-use reports that can be publicly shared, making them ideal for organizations that want to build trust with customers and stakeholders. SOC 3 reports are issued in two forms: SOC 3 Type 1 evaluates the design of controls at a specific point in time. SOC 3 Type 2 evaluates both the design and operational effectiveness of those controls over a defined period, typically 6 to 12 months. SOC 3 – Overview SOC 3 is a simplified, public version of SOC 2, providing the same level of assurance without disclosing detailed system information. It is suitable for organizations that want to demonstrate their commitment to data protection, service reliability, and operational transparency. SOC 3 is relevant for cloud service providers, data centers, SaaS platforms, and any organization managing customer data. It helps build market credibility and demonstrates alignment with global best practices in system controls and risk management. SOC 3 Type 1 & Type 2 – Key Requirements Establish a control environment aligned with AICPA’s Trust Services Criteria. Document security policies, access management, and monitoring protocols. Implement system availability and backup processes. Protect data integrity through change management and processing accuracy. Ensure privacy and confidentiality in data handling and storage. Demonstrate how controls operate over time (Type 2) or at a point in time (Type 1). Maintain evidence logs and audit trails for verification. Periodically review and update controls for continual improvement. SOC 3 Implementation and Audit Support At Quality Asia Certification, we provide independent assessment and reporting for SOC 3 Type 1 and Type 2. Our experienced auditors evaluate control systems, review supporting evidence, and issue a formal SOC 3 report recognized by global stakeholders. We ensure full compliance with the AICPA framework, helping organizations validate their trustworthiness without disclosing sensitive internal details. The resulting report can be used on websites, proposals, and marketing material to demonstrate operational excellence and commitment to data protection. SOC 3 Certification Process Initial Readiness Review – Understand organizational objectives and scope of controls. Control Assessment – Review control design (Type 1) and operational effectiveness (Type 2). Audit Execution – Evaluate systems against Trust Services Criteria. Report Issuance – Provide a final SOC 3 report suitable for public distribution. Ongoing Surveillance – Reassessment in future periods to maintain assurance continuity.   Contact Quality Asia for SOC 3 Certification If your organization aims to demonstrate secure and trustworthy operations to customers, partners, or the public, SOC 3 certification can help. Quality Asia Certification offers comprehensive SOC 3 Type 1 and Type 2 assessment and reporting in accordance with AICPA guidelines. Strengthen your brand’s reputation, ensure regulatory alignment, and assure stakeholders with a globally accepted SOC 3 report.
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  • soc 3 certification consultancy

    soc 3 certification consultancy

    25,000 / Set

    What is SOC 3 Type 1 & Type 2? SOC 3 (System and Organization Controls 3) reports are designed to assure the public about the integrity and security of a service organization 's systems. Based on the AICPA Trust Services Criteria, SOC 3 evaluates controls related to Security, Availability, Processing Integrity, Confidentiality, and Privacy. Unlike SOC 2, SOC 3 reports are general-use reports that can be publicly shared, making them ideal for organizations that want to build trust with customers and stakeholders. SOC 3 reports are issued in two forms: SOC 3 Type 1 evaluates the design of controls at a specific point in time. SOC 3 Type 2 evaluates both the design and operational effectiveness of those controls over a defined period, typically 6 to 12 months. SOC 3 – Overview SOC 3 is a simplified, public version of SOC 2, providing the same level of assurance without disclosing detailed system information. It is suitable for organizations that want to demonstrate their commitment to data protection, service reliability, and operational transparency. SOC 3 is relevant for cloud service providers, data centers, SaaS platforms, and any organization managing customer data. It helps build market credibility and demonstrates alignment with global best practices in system controls and risk management. SOC 3 Type 1 & Type 2 – Key Requirements Establish a control environment aligned with AICPA’s Trust Services Criteria. Document security policies, access management, and monitoring protocols. Implement system availability and backup processes. Protect data integrity through change management and processing accuracy. Ensure privacy and confidentiality in data handling and storage. Demonstrate how controls operate over time (Type 2) or at a point in time (Type 1). Maintain evidence logs and audit trails for verification. Periodically review and update controls for continual improvement. SOC 3 Implementation and Audit Support At Quality Asia Certification, we provide independent assessment and reporting for SOC 3 Type 1 and Type 2. Our experienced auditors evaluate control systems, review supporting evidence, and issue a formal SOC 3 report recognized by global stakeholders. We ensure full compliance with the AICPA framework, helping organizations validate their trustworthiness without disclosing sensitive internal details. The resulting report can be used on websites, proposals, and marketing material to demonstrate operational excellence and commitment to data protection. SOC 3 Certification Process Initial Readiness Review – Understand organizational objectives and scope of controls. Control Assessment – Review control design (Type 1) and operational effectiveness (Type 2). Audit Execution – Evaluate systems against Trust Services Criteria. Report Issuance – Provide a final SOC 3 report suitable for public distribution. Ongoing Surveillance – Reassessment in future periods to maintain assurance continuity.   Contact Quality Asia for SOC 3 Certification If your organization aims to demonstrate secure and trustworthy operations to customers, partners, or the public, SOC 3 certification can help. Quality Asia Certification offers comprehensive SOC 3 Type 1 and Type 2 assessment and reporting in accordance with AICPA guidelines. Strengthen your brand’s reputation, ensure regulatory alignment, and assure stakeholders with a globally accepted SOC 3 report.

    Brand Name : SOC-3 Type 1,2 Report

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  • Soc 2 Type 2 Certification Service

    Soc 2 Type 2 Certification Service

    25,000 / Set

    • Country of OriginIndia
    • TypeSOC-2 Type 1, 2
    • What is SOC 2 Type I & Type II? SOC 2 (System and Organization Controls 2) is a globally recognized framework developed by the American Institute of Certified Public Accountants (AICPA) for managing customer data based on five trust service principles: security, availability, processing integrity, confidentiality, and privacy. SOC 2 reports are essential for technology-driven and cloud-based companies that handle sensitive customer information. SOC 2 Type I evaluates the design and implementation of controls at a specific point in time. It provides a snapshot of whether systems and controls are properly designed to meet trust principles. SOC 2 Type II assesses the operational effectiveness of those controls over a defined period, typically 3 to 12 months, offering deeper assurance of ongoing compliance. The latest guidance for SOC 2 is aligned with the 2017 Trust Services Criteria, updated by AICPA to reflect modern risks, including cybersecurity and data privacy. SOC 2 – Overview SOC 2 certification is not a one-size-fits-all approach. Each report is tailored to the specific systems and controls relevant to the organization’s operations. It is widely adopted by SaaS providers, fintech firms, IT service companies, and any business handling cloud data. SOC 2 strengthens customer trust by demonstrating that adequate internal controls are in place and consistently maintained to safeguard data and ensure service reliability. SOC 2 Trust Principles Covered Security – Protection of systems against unauthorized access and breaches. Availability – Ensuring systems are available for use as agreed upon. Processing Integrity – Guaranteeing data is processed accurately and completely. Confidentiality – Protecting sensitive information from unauthorized disclosure. Privacy – Managing personal data in accordance with recognized privacy policies. SOC 2 Type I & II Certification Scope Defines the organization’s system boundaries, components, services, and control environment. Outlines policies, procedures, and technical controls relevant to the selected trust principles. Establishes evidence of system design (Type I) and ongoing operation (Type II). Supports regulatory, customer, and contractual requirements for third-party assurance. Delivers a detailed independent audit report to be shared with stakeholders. Benefits of SOC 2 Certification Enhances trust with clients, partners, and regulators. Demonstrates robust information security and risk management practices. Improves internal processes and control monitoring. Strengthens competitive positioning, especially in data-sensitive markets. Reduces potential legal and financial liabilities associated with data breaches. Ensures alignment with industry-leading security and compliance standards.   Why Choose Quality Asia Certification At Quality Asia Certification, we issue globally trusted SOC 2 Type I & Type II reports following rigorous audit methodologies. Our reports provide evidence of your system’s reliability and data protection capabilities. With a deep understanding of cloud-based and IT-enabled environments, we assess your organization’s readiness and validate control effectiveness in alignment with the Trust Services Criteria. Our process ensures integrity, transparency, and credibility in every SOC 2 engagement.
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  • Soc 2 Type 2 Certification Service

    Soc 2 Type 2 Certification Service

    25,000 / Set

    What is SOC 2 Type I & Type II? SOC 2 (System and Organization Controls 2) is a globally recognized framework developed by the American Institute of Certified Public Accountants (AICPA) for managing customer data based on five trust service principles: security, availability, processing integrity, confidentiality, and privacy. SOC 2 reports are essential for technology-driven and cloud-based companies that handle sensitive customer information. SOC 2 Type I evaluates the design and implementation of controls at a specific point in time. It provides a snapshot of whether systems and controls are properly designed to meet trust principles. SOC 2 Type II assesses the operational effectiveness of those controls over a defined period, typically 3 to 12 months, offering deeper assurance of ongoing compliance. The latest guidance for SOC 2 is aligned with the 2017 Trust Services Criteria, updated by AICPA to reflect modern risks, including cybersecurity and data privacy. SOC 2 – Overview SOC 2 certification is not a one-size-fits-all approach. Each report is tailored to the specific systems and controls relevant to the organization’s operations. It is widely adopted by SaaS providers, fintech firms, IT service companies, and any business handling cloud data. SOC 2 strengthens customer trust by demonstrating that adequate internal controls are in place and consistently maintained to safeguard data and ensure service reliability. SOC 2 Trust Principles Covered Security – Protection of systems against unauthorized access and breaches. Availability – Ensuring systems are available for use as agreed upon. Processing Integrity – Guaranteeing data is processed accurately and completely. Confidentiality – Protecting sensitive information from unauthorized disclosure. Privacy – Managing personal data in accordance with recognized privacy policies. SOC 2 Type I & II Certification Scope Defines the organization’s system boundaries, components, services, and control environment. Outlines policies, procedures, and technical controls relevant to the selected trust principles. Establishes evidence of system design (Type I) and ongoing operation (Type II). Supports regulatory, customer, and contractual requirements for third-party assurance. Delivers a detailed independent audit report to be shared with stakeholders. Benefits of SOC 2 Certification Enhances trust with clients, partners, and regulators. Demonstrates robust information security and risk management practices. Improves internal processes and control monitoring. Strengthens competitive positioning, especially in data-sensitive markets. Reduces potential legal and financial liabilities associated with data breaches. Ensures alignment with industry-leading security and compliance standards.   Why Choose Quality Asia Certification At Quality Asia Certification, we issue globally trusted SOC 2 Type I & Type II reports following rigorous audit methodologies. Our reports provide evidence of your system’s reliability and data protection capabilities. With a deep understanding of cloud-based and IT-enabled environments, we assess your organization’s readiness and validate control effectiveness in alignment with the Trust Services Criteria. Our process ensures integrity, transparency, and credibility in every SOC 2 engagement.

    Country of Origin : India

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  • soc 1 type 2 certification service

    soc 1 type 2 certification service

    25,000 / Numbers

    • Number Of FlowerSOC-1 Type 1, 2
    • Duration20 days
    • What is SOC 1 Type I & Type II Report (SSAE 18:2023)? SOC 1 (System and Organization Controls) Type I and Type II reports are part of the AICPA 's SSAE 18 standard, revised in 2023, focused on internal control reporting for service organizations that impact their clients’ financial reporting. These reports are essential for companies that provide outsourced services—such as payroll processing, data hosting, or billing—to demonstrate that their internal controls are suitably designed (Type I) and operating effectively over time (Type II). SOC 1 is primarily used by auditors and clients to gain assurance over control environments that affect financial data. SOC 1 Type I & Type II – Overview SOC 1 Type I evaluates the design and implementation of internal controls as of a specific date. It confirms whether the controls are suitably designed to achieve their control objectives. SOC 1 Type II goes further by assessing the operating effectiveness of those controls over a defined review period, usually 6 to 12 months. Both reports are structured according to the SSAE 18 framework issued by the American Institute of Certified Public Accountants (AICPA). These reports are widely recognized in regulated industries, including finance, insurance, and IT-enabled services. SOC 1 Reporting Scope and Control Areas Define the system and services relevant to user entity financial reporting. Identify and document control objectives and related controls. Implement access control, change management, data integrity, and process monitoring. Ensure proper segregation of duties and system availability controls. Provide supporting documentation, evidence logs, and risk mitigation practices. Maintain formal policies for incident management, backup, and recovery processes. Benefits of SOC 1 Type I & Type II Reports Builds client confidence by demonstrating reliable internal control systems. Enhances credibility during client audits and vendor assessments. Reduces the need for multiple client audits or questionnaires. Mitigates financial reporting risks and promotes regulatory compliance. Improves organizational transparency and accountability. Strengthens trust with financial institutions and enterprise clients. Supports long-term contracts by fulfilling third-party assurance requirements. SOC 1 Type I & Type II Report Process Readiness Assessment – Review existing control documentation and identify areas for improvement. Control Documentation – Define system boundaries, services, and control objectives. Evidence Collection – Gather records that support design and operation of controls. Type I Report – Evaluate and report on the design of controls at a point in time. Type II Report – Review operational effectiveness of controls over a 6–12 month period. Final Issuance – Receive an independent assurance report detailing control reliability and effectiveness.   Get SOC 1 Assurance with Quality Asia Certification If your organization delivers services that impact client financial reporting, obtaining a SOC 1 report under SSAE 18:2023 demonstrates your commitment to operational excellence and financial accuracy. Quality Asia Certification supports you in obtaining independent SOC 1 Type I and Type II reports, helping your business meet client demands and industry expectations. With a focus on confidentiality, integrity, and compliance, we ensure that your control environment stands up to scrutiny and supports continued growth.
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  • soc 1 type 2 certification service

    soc 1 type 2 certification service

    25,000 / Numbers

    What is SOC 1 Type I & Type II Report (SSAE 18:2023)? SOC 1 (System and Organization Controls) Type I and Type II reports are part of the AICPA 's SSAE 18 standard, revised in 2023, focused on internal control reporting for service organizations that impact their clients’ financial reporting. These reports are essential for companies that provide outsourced services—such as payroll processing, data hosting, or billing—to demonstrate that their internal controls are suitably designed (Type I) and operating effectively over time (Type II). SOC 1 is primarily used by auditors and clients to gain assurance over control environments that affect financial data. SOC 1 Type I & Type II – Overview SOC 1 Type I evaluates the design and implementation of internal controls as of a specific date. It confirms whether the controls are suitably designed to achieve their control objectives. SOC 1 Type II goes further by assessing the operating effectiveness of those controls over a defined review period, usually 6 to 12 months. Both reports are structured according to the SSAE 18 framework issued by the American Institute of Certified Public Accountants (AICPA). These reports are widely recognized in regulated industries, including finance, insurance, and IT-enabled services. SOC 1 Reporting Scope and Control Areas Define the system and services relevant to user entity financial reporting. Identify and document control objectives and related controls. Implement access control, change management, data integrity, and process monitoring. Ensure proper segregation of duties and system availability controls. Provide supporting documentation, evidence logs, and risk mitigation practices. Maintain formal policies for incident management, backup, and recovery processes. Benefits of SOC 1 Type I & Type II Reports Builds client confidence by demonstrating reliable internal control systems. Enhances credibility during client audits and vendor assessments. Reduces the need for multiple client audits or questionnaires. Mitigates financial reporting risks and promotes regulatory compliance. Improves organizational transparency and accountability. Strengthens trust with financial institutions and enterprise clients. Supports long-term contracts by fulfilling third-party assurance requirements. SOC 1 Type I & Type II Report Process Readiness Assessment – Review existing control documentation and identify areas for improvement. Control Documentation – Define system boundaries, services, and control objectives. Evidence Collection – Gather records that support design and operation of controls. Type I Report – Evaluate and report on the design of controls at a point in time. Type II Report – Review operational effectiveness of controls over a 6–12 month period. Final Issuance – Receive an independent assurance report detailing control reliability and effectiveness.   Get SOC 1 Assurance with Quality Asia Certification If your organization delivers services that impact client financial reporting, obtaining a SOC 1 report under SSAE 18:2023 demonstrates your commitment to operational excellence and financial accuracy. Quality Asia Certification supports you in obtaining independent SOC 1 Type I and Type II reports, helping your business meet client demands and industry expectations. With a focus on confidentiality, integrity, and compliance, we ensure that your control environment stands up to scrutiny and supports continued growth.

    Number Of Flower : SOC-1 Type 1, 2

    Duration : 20 days

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  • ISO 9950 Certification Service

    ISO 9950 Certification Service

    25,000 / Set

    • Type of CertificationISO 9950
    • Industry FocusDiverse
    • Certification Body AccreditationNABCB
    • Implementation Timeline20 days
    • CostBased On Company Size & Complexity
    • ISO 9950:2007 Certification for Industrial Furnaces – Surface Temperature Uniformity Overview ISO 9950:2007 is an international standard that specifies the method for measuring the surface temperature uniformity of furnace linings in industrial furnaces. This standard is crucial in ensuring that industrial furnaces maintain consistent temperature distribution on the inner surfaces of their working chambers. Maintaining such uniformity is essential for improving process efficiency, energy consumption, product quality, and safety in various heat-treatment operations. What is ISO 9950:2007? ISO 9950:2007 titled “Industrial furnaces and associated processing equipment — Measurement of surface temperature uniformity of the furnace lining” outlines procedures to assess and validate the surface temperature uniformity of furnace linings during operation. The surface temperature is a critical factor in industrial heating processes, affecting material properties and energy efficiency. The standard applies to both new and existing furnaces and is relevant to industries involved in heat treatment, metallurgy, ceramics, and manufacturing of high-temperature equipment. Why ISO 9950:2007 Certification? Industries seek ISO 9950:2007 certification to demonstrate their compliance with global best practices in temperature measurement and furnace maintenance. Achieving this certification ensures that organizations maintain controlled temperature environments that are critical for precise material processing. It minimizes the risk of defects in the final product and optimizes energy usage. Certification also signifies the organization 's commitment to maintaining safety standards and operational excellence in high-temperature environments. Requirements for ISO 9950:2007 Certification To comply with ISO 9950:2007, organizations must: Conduct temperature mapping and surface temperature measurements as per the standard’s protocol. Ensure appropriate placement of measurement instruments such as thermocouples or infrared sensors. Prepare documentation detailing furnace design, operation modes, and thermal characteristics. Maintain a record of test results and calibration certificates for measurement equipment. Implement corrective actions in case non-uniformities exceed acceptable limits. Schedule periodic assessments to ensure ongoing compliance and performance. Certification Process Application Submission: Organization submits a request for ISO 9950:2007 certification. Document Review: Evaluation of furnace-related documentation including design, operational records, and previous test reports. On-site Assessment: An audit is conducted to measure surface temperature uniformity using approved methods. Non-conformity Closure: Any deviations identified during the audit must be addressed and resolved. Issuance of Certificate: Upon successful evaluation, ISO 9950:2007 certification is issued with a defined validity period. Surveillance Audits: Regular follow-ups are conducted to ensure ongoing compliance with the standard. Benefits of ISO 9950:2007 Certification   Ensures uniform heat distribution in furnaces, improving product quality. Reduces energy consumption and operational inefficiencies. Minimizes risk of material deformation or damage due to uneven temperatures. Supports regulatory and industry compliance for furnace operation. Enhances reliability and longevity of furnace linings and components. Improves safety conditions for operators by maintaining controlled thermal environments.
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  • ISO 9950 Certification Service

    ISO 9950 Certification Service

    25,000 / Set

    ISO 9950:2007 Certification for Industrial Furnaces – Surface Temperature Uniformity Overview ISO 9950:2007 is an international standard that specifies the method for measuring the surface temperature uniformity of furnace linings in industrial furnaces. This standard is crucial in ensuring that industrial furnaces maintain consistent temperature distribution on the inner surfaces of their working chambers. Maintaining such uniformity is essential for improving process efficiency, energy consumption, product quality, and safety in various heat-treatment operations. What is ISO 9950:2007? ISO 9950:2007 titled “Industrial furnaces and associated processing equipment — Measurement of surface temperature uniformity of the furnace lining” outlines procedures to assess and validate the surface temperature uniformity of furnace linings during operation. The surface temperature is a critical factor in industrial heating processes, affecting material properties and energy efficiency. The standard applies to both new and existing furnaces and is relevant to industries involved in heat treatment, metallurgy, ceramics, and manufacturing of high-temperature equipment. Why ISO 9950:2007 Certification? Industries seek ISO 9950:2007 certification to demonstrate their compliance with global best practices in temperature measurement and furnace maintenance. Achieving this certification ensures that organizations maintain controlled temperature environments that are critical for precise material processing. It minimizes the risk of defects in the final product and optimizes energy usage. Certification also signifies the organization 's commitment to maintaining safety standards and operational excellence in high-temperature environments. Requirements for ISO 9950:2007 Certification To comply with ISO 9950:2007, organizations must: Conduct temperature mapping and surface temperature measurements as per the standard’s protocol. Ensure appropriate placement of measurement instruments such as thermocouples or infrared sensors. Prepare documentation detailing furnace design, operation modes, and thermal characteristics. Maintain a record of test results and calibration certificates for measurement equipment. Implement corrective actions in case non-uniformities exceed acceptable limits. Schedule periodic assessments to ensure ongoing compliance and performance. Certification Process Application Submission: Organization submits a request for ISO 9950:2007 certification. Document Review: Evaluation of furnace-related documentation including design, operational records, and previous test reports. On-site Assessment: An audit is conducted to measure surface temperature uniformity using approved methods. Non-conformity Closure: Any deviations identified during the audit must be addressed and resolved. Issuance of Certificate: Upon successful evaluation, ISO 9950:2007 certification is issued with a defined validity period. Surveillance Audits: Regular follow-ups are conducted to ensure ongoing compliance with the standard. Benefits of ISO 9950:2007 Certification   Ensures uniform heat distribution in furnaces, improving product quality. Reduces energy consumption and operational inefficiencies. Minimizes risk of material deformation or damage due to uneven temperatures. Supports regulatory and industry compliance for furnace operation. Enhances reliability and longevity of furnace linings and components. Improves safety conditions for operators by maintaining controlled thermal environments.

    Type of Certification : ISO 9950

    Industry Focus : Diverse

    Certification Body Accreditation : NABCB

    Implementation Timeline : 20 days

    Cost : Based On Company Size & Complexity

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  • ISO 9328 Certification Service

    ISO 9328 Certification Service

    25,000 / Set

    • Type of CertificationISO 9328
    • Industry FocusDiverse
    • Certification Body AccreditationNABCB
    • Implementation Timeline20 days
    • CostBased On Company Size & Complexity
    • What is ISO 9328:2018? ISO 9328:2018 is a series of international standards that specify the technical delivery conditions for steel plates and strips used under pressure and in general applications. The standard outlines requirements for different grades of weldable steels suitable for pressure vessels and other industrial uses. It ensures consistency in chemical composition, mechanical properties, and testing procedures, helping manufacturers and end-users maintain quality and safety in steel products subjected to high stress or pressure. ISO 9328 – Overview The ISO 9328 series is divided into multiple parts, with each part addressing a specific grade or type of steel used in pressure applications. These include fine-grain steels, normalized or thermomechanically rolled steels, and alloyed or non-alloyed steels. The standard provides guidance on delivery conditions, testing methods, and acceptance criteria. It is widely used in industries such as petrochemicals, power generation, shipbuilding, and heavy machinery, where reliable and high-performance steel is essential for safe operation. ISO 9328:2018 Key Requirements Specify steel grades and mechanical properties such as yield strength, tensile strength, and elongation. Ensure proper chemical composition with defined limits for carbon, manganese, sulfur, phosphorus, and other alloying elements. Comply with heat treatment conditions like normalizing or quenching and tempering. Meet dimensional tolerances, flatness, and surface quality requirements. Conduct mandatory testing including tensile tests, impact tests, and ultrasonic inspections. Apply clear identification markings and traceability of steel plates and coils. Maintain complete documentation such as mill test certificates and compliance reports. Follow specified procedures for sampling and product verification. ISO 9328 Certification with Quality Asia Certification Quality Asia Certification offers ISO 9328:2018 certification services to manufacturers of steel plates, strips, and coils intended for pressure equipment and structural use. Certification verifies that the products meet international quality and safety standards, ensuring reliable performance in critical applications. It also strengthens confidence among buyers, regulators, and engineering firms regarding the material 's suitability for demanding environments. Certification Process for ISO 9328 Application Review – Evaluation of the steel product type, grade, and intended use. Stage 1 Audit – Review of quality control systems, test records, and documentation. Stage 2 Audit – On-site assessment of manufacturing processes, inspection systems, and compliance with standard requirements. Certification Decision – Granting of ISO 9328 certification after successful audit closure. Surveillance Audits – Annual evaluations to maintain compliance and product consistency. Recertification – Comprehensive reassessment every three years to renew certification. Benefits of ISO 9328 Certification Ensures product compliance with international pressure equipment standards. Improves reliability and safety in high-pressure and structural applications. Supports access to global markets with recognized certification. Enhances customer trust through verified steel quality and testing practices. Reduces risk of failure and non-conformance in mission-critical environments. Promotes transparent documentation and traceability of steel materials.   Get ISO 9328 Certified with Us If your organization manufactures steel plates or strips for pressure equipment or structural applications, ISO 9328:2018 certification ensures that your products meet global expectations for safety and performance. Quality Asia Certification offers internationally recognized certification services tailored to your industry requirements. Contact us today to begin your ISO 9328 certification journey.
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  • ISO 9328 Certification Service

    ISO 9328 Certification Service

    25,000 / Set

    What is ISO 9328:2018? ISO 9328:2018 is a series of international standards that specify the technical delivery conditions for steel plates and strips used under pressure and in general applications. The standard outlines requirements for different grades of weldable steels suitable for pressure vessels and other industrial uses. It ensures consistency in chemical composition, mechanical properties, and testing procedures, helping manufacturers and end-users maintain quality and safety in steel products subjected to high stress or pressure. ISO 9328 – Overview The ISO 9328 series is divided into multiple parts, with each part addressing a specific grade or type of steel used in pressure applications. These include fine-grain steels, normalized or thermomechanically rolled steels, and alloyed or non-alloyed steels. The standard provides guidance on delivery conditions, testing methods, and acceptance criteria. It is widely used in industries such as petrochemicals, power generation, shipbuilding, and heavy machinery, where reliable and high-performance steel is essential for safe operation. ISO 9328:2018 Key Requirements Specify steel grades and mechanical properties such as yield strength, tensile strength, and elongation. Ensure proper chemical composition with defined limits for carbon, manganese, sulfur, phosphorus, and other alloying elements. Comply with heat treatment conditions like normalizing or quenching and tempering. Meet dimensional tolerances, flatness, and surface quality requirements. Conduct mandatory testing including tensile tests, impact tests, and ultrasonic inspections. Apply clear identification markings and traceability of steel plates and coils. Maintain complete documentation such as mill test certificates and compliance reports. Follow specified procedures for sampling and product verification. ISO 9328 Certification with Quality Asia Certification Quality Asia Certification offers ISO 9328:2018 certification services to manufacturers of steel plates, strips, and coils intended for pressure equipment and structural use. Certification verifies that the products meet international quality and safety standards, ensuring reliable performance in critical applications. It also strengthens confidence among buyers, regulators, and engineering firms regarding the material 's suitability for demanding environments. Certification Process for ISO 9328 Application Review – Evaluation of the steel product type, grade, and intended use. Stage 1 Audit – Review of quality control systems, test records, and documentation. Stage 2 Audit – On-site assessment of manufacturing processes, inspection systems, and compliance with standard requirements. Certification Decision – Granting of ISO 9328 certification after successful audit closure. Surveillance Audits – Annual evaluations to maintain compliance and product consistency. Recertification – Comprehensive reassessment every three years to renew certification. Benefits of ISO 9328 Certification Ensures product compliance with international pressure equipment standards. Improves reliability and safety in high-pressure and structural applications. Supports access to global markets with recognized certification. Enhances customer trust through verified steel quality and testing practices. Reduces risk of failure and non-conformance in mission-critical environments. Promotes transparent documentation and traceability of steel materials.   Get ISO 9328 Certified with Us If your organization manufactures steel plates or strips for pressure equipment or structural applications, ISO 9328:2018 certification ensures that your products meet global expectations for safety and performance. Quality Asia Certification offers internationally recognized certification services tailored to your industry requirements. Contact us today to begin your ISO 9328 certification journey.

    Type of Certification : ISO 9328

    Industry Focus : Diverse

    Certification Body Accreditation : NABCB

    Implementation Timeline : 20 days

    Cost : Based On Company Size & Complexity

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  • ISO 9241 Certification Service

    ISO 9241 Certification Service

    25,000 / Number

    • CostBased On Company Size & Complexity
    • Implementation Timeline20 Days
    • Certification Body AccreditationNABCB
    • Company SizeALL
    • Type of CertificationISO 9241
    • What is ISO 9241:2010? ISO 9241:2010 is a globally recognized standard focused on ergonomics and usability in the interaction between humans and computer systems. It provides detailed guidelines to ensure that products, systems, and services are designed for effective, efficient, and user-friendly experiences. Originally developed for office work with visual display terminals, ISO 9241 has evolved into a comprehensive standard that now addresses human-system interaction across hardware, software, and user environments. ISO 9241 – Overview ISO 9241:2010 consists of multiple parts covering ergonomics principles, visual display requirements, input device usability, and software interface design. It helps organizations develop systems that meet user needs while reducing errors, fatigue, and health risks. This standard is applicable across industries where human-machine interaction plays a key role—such as IT, manufacturing, healthcare, aviation, automotive, and more. Implementing ISO 9241 demonstrates a commitment to user safety, accessibility, and productivity, ultimately enhancing the overall quality of systems and services. ISO 9241:2010 Key Focus Areas Design principles for user interfaces and system usability. Requirements for displays, keyboards, and input devices. Guidelines for software dialogues and task efficiency. Visual ergonomics including lighting, screen readability, and viewing angles. User feedback and interactive response timing. Minimizing user workload and cognitive strain. Ensuring accessibility and inclusivity in system design. Training and Implementation Alignment Organizations applying ISO 9241 integrate ergonomic principles into system development and workplace environments. It supports the creation of user-centric designs that improve safety, performance, and satisfaction. The standard can be applied during the design, evaluation, and testing phases of both hardware and software products. ISO 9241 also aligns with quality management practices by ensuring systems are usable, maintainable, and meet the expectations of diverse users, including those with disabilities. Certification Preparation Process Gap Identification – Evaluate current system design, interfaces, and workplace ergonomics. Policy and Procedure Development – Define guidelines for human-system interaction, input devices, and display configurations. System Design Review – Assess usability, accessibility, and comfort across various user scenarios. Validation and Documentation – Conduct usability testing and document compliance evidence. Readiness Evaluation – Prepare for external audits through internal reviews and system refinements. Why Choose ISO 9241 Certification? Enhances product and system usability across platforms. Improves safety and comfort in workplace environments. Reduces risk of repetitive strain injuries and visual fatigue. Supports inclusive design practices for all user groups. Boosts customer confidence and brand reputation through ergonomic excellence. Ensures compliance with international standards in human-system interaction. Apply for ISO 9241 Certification If your organization is committed to improving usability, accessibility, and ergonomics in its systems, ISO 9241:2010 certification is a valuable step. Quality Asia Certification offers globally recognized ISO 9241 certification services to help organizations meet industry benchmarks in human-centered design. Achieve higher user satisfaction, improved safety, and increased system efficiency through structured and validated practices.
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  • ISO 9241 Certification Service

    ISO 9241 Certification Service

    25,000 / Number

    What is ISO 9241:2010? ISO 9241:2010 is a globally recognized standard focused on ergonomics and usability in the interaction between humans and computer systems. It provides detailed guidelines to ensure that products, systems, and services are designed for effective, efficient, and user-friendly experiences. Originally developed for office work with visual display terminals, ISO 9241 has evolved into a comprehensive standard that now addresses human-system interaction across hardware, software, and user environments. ISO 9241 – Overview ISO 9241:2010 consists of multiple parts covering ergonomics principles, visual display requirements, input device usability, and software interface design. It helps organizations develop systems that meet user needs while reducing errors, fatigue, and health risks. This standard is applicable across industries where human-machine interaction plays a key role—such as IT, manufacturing, healthcare, aviation, automotive, and more. Implementing ISO 9241 demonstrates a commitment to user safety, accessibility, and productivity, ultimately enhancing the overall quality of systems and services. ISO 9241:2010 Key Focus Areas Design principles for user interfaces and system usability. Requirements for displays, keyboards, and input devices. Guidelines for software dialogues and task efficiency. Visual ergonomics including lighting, screen readability, and viewing angles. User feedback and interactive response timing. Minimizing user workload and cognitive strain. Ensuring accessibility and inclusivity in system design. Training and Implementation Alignment Organizations applying ISO 9241 integrate ergonomic principles into system development and workplace environments. It supports the creation of user-centric designs that improve safety, performance, and satisfaction. The standard can be applied during the design, evaluation, and testing phases of both hardware and software products. ISO 9241 also aligns with quality management practices by ensuring systems are usable, maintainable, and meet the expectations of diverse users, including those with disabilities. Certification Preparation Process Gap Identification – Evaluate current system design, interfaces, and workplace ergonomics. Policy and Procedure Development – Define guidelines for human-system interaction, input devices, and display configurations. System Design Review – Assess usability, accessibility, and comfort across various user scenarios. Validation and Documentation – Conduct usability testing and document compliance evidence. Readiness Evaluation – Prepare for external audits through internal reviews and system refinements. Why Choose ISO 9241 Certification? Enhances product and system usability across platforms. Improves safety and comfort in workplace environments. Reduces risk of repetitive strain injuries and visual fatigue. Supports inclusive design practices for all user groups. Boosts customer confidence and brand reputation through ergonomic excellence. Ensures compliance with international standards in human-system interaction. Apply for ISO 9241 Certification If your organization is committed to improving usability, accessibility, and ergonomics in its systems, ISO 9241:2010 certification is a valuable step. Quality Asia Certification offers globally recognized ISO 9241 certification services to help organizations meet industry benchmarks in human-centered design. Achieve higher user satisfaction, improved safety, and increased system efficiency through structured and validated practices.

    Cost : Based On Company Size & Complexity

    Implementation Timeline : 20 Days

    Certification Body Accreditation : NABCB

    Company Size : ALL

    Type of Certification : ISO 9241

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  • ISO 9202 Certification Service

    ISO 9202 Certification Service

    25,000 / Set

    • Type of CertificationISO 9202
    • Industry FocusDiverse
    • Certification Body AccreditationNABCB
    • Implementation Timeline20 days
    • CostBased On Company Size & Complexity
    • ISO 9202:2019 Certification – Jewellery Vocabulary Standard Overview ISO 9202:2019 specifies a vocabulary of terms used in the jewellery industry, particularly for precious metals and their alloys. This international standard supports clear communication across global markets by defining standardized terminology. It is essential for manufacturers, traders, certifying bodies, and regulators dealing with precious metal jewellery to ensure product authenticity, legal compliance, and quality control. What is ISO 9202:2019? ISO 9202:2019 is the latest version of the standard titled “Jewellery — Fineness of precious metal alloys.” It establishes definitions and standardized terms related to the fineness of gold, silver, platinum, and palladium used in jewellery. The standard outlines permissible tolerances and acceptable compositions, enabling consistency in global jewellery manufacturing and trade. It ensures that buyers, sellers, and regulators interpret terms like “karat,” “fineness,” or “plumb” consistently. Why This Product Jewellery businesses and hallmarking centers often face discrepancies due to inconsistent use of terminology across borders. ISO 9202:2019 resolves this issue by harmonizing terms related to precious metal alloys. Certification to ISO 9202 demonstrates that your organization adheres to globally recognized terminology, which reduces risk of misrepresentation and improves buyer trust. It also aligns your business with regulatory frameworks that reference ISO standards for precious metals. Benefits of ISO 9202:2019 Certification   Establishes standardized terminology for gold, silver, platinum, and palladium products Supports global trade by eliminating confusion over precious metal fineness Enhances brand trust through accurate labelling and terminology compliance Facilitates smoother communication between suppliers, retailers, and regulatory bodies Assists in quality assurance by clearly defining fineness tolerances and alloy compositions Reduces disputes and legal issues by providing a universally accepted vocabulary
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  • ISO 9202 Certification Service

    ISO 9202 Certification Service

    25,000 / Set

    ISO 9202:2019 Certification – Jewellery Vocabulary Standard Overview ISO 9202:2019 specifies a vocabulary of terms used in the jewellery industry, particularly for precious metals and their alloys. This international standard supports clear communication across global markets by defining standardized terminology. It is essential for manufacturers, traders, certifying bodies, and regulators dealing with precious metal jewellery to ensure product authenticity, legal compliance, and quality control. What is ISO 9202:2019? ISO 9202:2019 is the latest version of the standard titled “Jewellery — Fineness of precious metal alloys.” It establishes definitions and standardized terms related to the fineness of gold, silver, platinum, and palladium used in jewellery. The standard outlines permissible tolerances and acceptable compositions, enabling consistency in global jewellery manufacturing and trade. It ensures that buyers, sellers, and regulators interpret terms like “karat,” “fineness,” or “plumb” consistently. Why This Product Jewellery businesses and hallmarking centers often face discrepancies due to inconsistent use of terminology across borders. ISO 9202:2019 resolves this issue by harmonizing terms related to precious metal alloys. Certification to ISO 9202 demonstrates that your organization adheres to globally recognized terminology, which reduces risk of misrepresentation and improves buyer trust. It also aligns your business with regulatory frameworks that reference ISO standards for precious metals. Benefits of ISO 9202:2019 Certification   Establishes standardized terminology for gold, silver, platinum, and palladium products Supports global trade by eliminating confusion over precious metal fineness Enhances brand trust through accurate labelling and terminology compliance Facilitates smoother communication between suppliers, retailers, and regulatory bodies Assists in quality assurance by clearly defining fineness tolerances and alloy compositions Reduces disputes and legal issues by providing a universally accepted vocabulary

    Type of Certification : ISO 9202

    Industry Focus : Diverse

    Certification Body Accreditation : NABCB

    Implementation Timeline : 20 days

    Cost : Based On Company Size & Complexity

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  • ISO 9001 2015 Certification Services

    ISO 9001 2015 Certification Services

    25,000 / Number

    • Number Of FlowerISO 9001
    • AccreditationNABCB
    • Time15 days
    • What is ISO 9001 Quality Management System (QMS)? ISO 9001 is the internationally recognized standard for quality management systems. It is developed and maintained by the International Organization for Standardization (ISO) and is implemented by organizations worldwide to ensure the consistent quality of products and services. ISO 9001 helps businesses establish a structured system that enhances customer satisfaction, operational efficiency, and continual improvement. ISO 9001 Overview ISO 9001:2015 is based on seven fundamental quality management principles which enable organizations to improve processes, strengthen leadership, and build sustainable customer relationships: Customer Focus Leadership Engagement of People Process Approach Improvement Evidence-Based Decision Making Relationship Management At Quality Asia Certification, we emphasize these seven principles while assessing organizations for ISO 9001 certification. These principles guide organizations in achieving higher performance and greater consistency across all departments. Benefits of ISO 9001 Implementation Through ISO 9001 certification, organizations can experience a range of operational and strategic benefits, including: Enhanced customer satisfaction and trust Streamlined internal processes Increased efficiency and productivity Reduction in errors, waste, and rework Better employee engagement and clarity of roles Improved decision-making based on data Strengthened business reputation in domestic and international markets Our Approach to ISO 9001 At Quality Asia Certification, we align our services with three key operational pillars: Organize Processes Continually Improve Enhance Process Efficiency This approach enables companies to establish a structured and adaptable quality management system that meets both current and future business needs. ISO 9001 Certification Requirements To achieve ISO 9001 certification, an organization must meet specific requirements that include: Establishing and maintaining a documented quality management system Defining quality objectives and measuring performance against them Determining and controlling process interactions Ensuring resource availability and maintaining a conducive work environment Monitoring, analyzing, and evaluating performance Conducting internal audits and management reviews Taking corrective actions and focusing on continual improvement Clearly defined roles and responsibilities at all levels ISO 9001 Training Support Organizations seeking ISO 9001 certification may require internal awareness and understanding of the standard. Through structured training programs, individuals can: Learn about the ISO 9001:2015 standard Understand the quality management principles in depth Gain the skills to support implementation, auditing, and maintenance of the QMS Contribute effectively to the success of the certification journey ISO 9001 Certification by Quality Asia Certification Quality Asia Certification is committed to delivering ISO 9001 certification services with professionalism, transparency, and impartiality. Our process ensures compliance with the ISO 9001:2015 standard while helping clients demonstrate: Adherence to the ISO 9001 requirements Alignment with customer, statutory, and regulatory obligations A structured and documented approach to quality management A proactive culture of continuous improvement   An ISO 9001 certification from Quality Asia Certification establishes an organization’s dedication to quality, enhances its global credibility, and ensures a competitive advantage in the marketplace.
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  • ISO 9001 2015 Certification Services

    ISO 9001 2015 Certification Services

    25,000 / Number

    What is ISO 9001 Quality Management System (QMS)? ISO 9001 is the internationally recognized standard for quality management systems. It is developed and maintained by the International Organization for Standardization (ISO) and is implemented by organizations worldwide to ensure the consistent quality of products and services. ISO 9001 helps businesses establish a structured system that enhances customer satisfaction, operational efficiency, and continual improvement. ISO 9001 Overview ISO 9001:2015 is based on seven fundamental quality management principles which enable organizations to improve processes, strengthen leadership, and build sustainable customer relationships: Customer Focus Leadership Engagement of People Process Approach Improvement Evidence-Based Decision Making Relationship Management At Quality Asia Certification, we emphasize these seven principles while assessing organizations for ISO 9001 certification. These principles guide organizations in achieving higher performance and greater consistency across all departments. Benefits of ISO 9001 Implementation Through ISO 9001 certification, organizations can experience a range of operational and strategic benefits, including: Enhanced customer satisfaction and trust Streamlined internal processes Increased efficiency and productivity Reduction in errors, waste, and rework Better employee engagement and clarity of roles Improved decision-making based on data Strengthened business reputation in domestic and international markets Our Approach to ISO 9001 At Quality Asia Certification, we align our services with three key operational pillars: Organize Processes Continually Improve Enhance Process Efficiency This approach enables companies to establish a structured and adaptable quality management system that meets both current and future business needs. ISO 9001 Certification Requirements To achieve ISO 9001 certification, an organization must meet specific requirements that include: Establishing and maintaining a documented quality management system Defining quality objectives and measuring performance against them Determining and controlling process interactions Ensuring resource availability and maintaining a conducive work environment Monitoring, analyzing, and evaluating performance Conducting internal audits and management reviews Taking corrective actions and focusing on continual improvement Clearly defined roles and responsibilities at all levels ISO 9001 Training Support Organizations seeking ISO 9001 certification may require internal awareness and understanding of the standard. Through structured training programs, individuals can: Learn about the ISO 9001:2015 standard Understand the quality management principles in depth Gain the skills to support implementation, auditing, and maintenance of the QMS Contribute effectively to the success of the certification journey ISO 9001 Certification by Quality Asia Certification Quality Asia Certification is committed to delivering ISO 9001 certification services with professionalism, transparency, and impartiality. Our process ensures compliance with the ISO 9001:2015 standard while helping clients demonstrate: Adherence to the ISO 9001 requirements Alignment with customer, statutory, and regulatory obligations A structured and documented approach to quality management A proactive culture of continuous improvement   An ISO 9001 certification from Quality Asia Certification establishes an organization’s dedication to quality, enhances its global credibility, and ensures a competitive advantage in the marketplace.

    Number Of Flower : ISO 9001

    Accreditation : NABCB

    Time : 15 days

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  • ISO 8986 Certification Service

    ISO 8986 Certification Service

    25,000 / Set

    • Type of CertificationISO 8986
    • Industry FocusDiverse
    • Certification Body AccreditationNABCB
    • Implementation Timeline20 days
    • CostBased On Company Size & Complexity
    • What is ISO 8986-1:2020? ISO 8986-1:2020 is an international standard that specifies the properties and testing methods for poly(phenylene ether) (PPE) moulding and extrusion materials. This part of the standard focuses on unreinforced PPE materials and defines their classification and requirements based on standardized tests. PPE plastics are known for their high heat resistance, dimensional stability, and electrical insulation properties, making them suitable for a wide range of engineering applications. ISO 8986 – Overview ISO 8986-1:2020 provides a framework for identifying PPE thermoplastic materials based on their performance in standardized tests. The classification system is structured by property values such as melt flow rate, tensile strength, and impact resistance. These materials are commonly used in automotive components, electrical housings, and industrial parts due to their thermal performance and chemical resistance. The standard helps manufacturers, suppliers, and product designers ensure consistent quality and functionality of PPE products across different applications and markets. ISO 8986:2020 Key Requirements Classify PPE materials based on their melt mass-flow rate (MFR), mechanical strength, and impact properties. Ensure standard test conditions, including sample preparation and environmental control during testing. Evaluate physical properties like density, tensile strength, elongation at break, and flexural modulus. Assess thermal properties such as heat deflection temperature and Vicat softening temperature. Measure electrical insulation performance and flammability where applicable. Use color coding and designation systems as per ISO guidelines for material identification. Ensure batch traceability, quality control records, and standardized markings on packaging or product. Adopt appropriate handling and storage practices to preserve material integrity. ISO 8986 Certification with Quality Asia Certification Quality Asia Certification offers ISO 8986-1:2020 certification services to manufacturers and suppliers of unreinforced PPE materials. Certification validates that the poly(phenylene ether) materials meet globally recognized specifications for mechanical, thermal, and physical performance. It ensures that your products align with international expectations for reliability and material classification in technical applications. Certification Process for ISO 8986 Application Review – Evaluation of PPE material types, grades, and usage scope. Stage 1 Audit – Review of testing data, quality assurance protocols, and technical documentation. Stage 2 Audit – On-site verification of processing methods, material identification, and test equipment. Certification Decision – Issuance of ISO 8986-1:2020 certificate after successful audit and compliance confirmation. Surveillance Audits – Yearly evaluations to maintain ongoing conformity and material performance consistency. Recertification – Complete reassessment every three years to ensure continued certification. Benefits of ISO 8986 Certification Ensures standardized quality and classification of PPE materials. Supports product development in high-performance plastic applications. Improves customer trust and acceptance in regulated markets. Reduces variability in material performance across production batches. Promotes transparency and traceability in material selection. Demonstrates compliance with international material testing standards. Get ISO 8986 Certified with Us If your organization produces or supplies unreinforced PPE materials for moulding and extrusion, ISO 8986-1:2020 certification confirms material compliance and quality consistency. Quality Asia Certification offers reliable ISO certification services to help your products meet international market standards. Contact us today to begin your ISO 8986 certification process.
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  • ISO 8986 Certification Service

    ISO 8986 Certification Service

    25,000 / Set

    What is ISO 8986-1:2020? ISO 8986-1:2020 is an international standard that specifies the properties and testing methods for poly(phenylene ether) (PPE) moulding and extrusion materials. This part of the standard focuses on unreinforced PPE materials and defines their classification and requirements based on standardized tests. PPE plastics are known for their high heat resistance, dimensional stability, and electrical insulation properties, making them suitable for a wide range of engineering applications. ISO 8986 – Overview ISO 8986-1:2020 provides a framework for identifying PPE thermoplastic materials based on their performance in standardized tests. The classification system is structured by property values such as melt flow rate, tensile strength, and impact resistance. These materials are commonly used in automotive components, electrical housings, and industrial parts due to their thermal performance and chemical resistance. The standard helps manufacturers, suppliers, and product designers ensure consistent quality and functionality of PPE products across different applications and markets. ISO 8986:2020 Key Requirements Classify PPE materials based on their melt mass-flow rate (MFR), mechanical strength, and impact properties. Ensure standard test conditions, including sample preparation and environmental control during testing. Evaluate physical properties like density, tensile strength, elongation at break, and flexural modulus. Assess thermal properties such as heat deflection temperature and Vicat softening temperature. Measure electrical insulation performance and flammability where applicable. Use color coding and designation systems as per ISO guidelines for material identification. Ensure batch traceability, quality control records, and standardized markings on packaging or product. Adopt appropriate handling and storage practices to preserve material integrity. ISO 8986 Certification with Quality Asia Certification Quality Asia Certification offers ISO 8986-1:2020 certification services to manufacturers and suppliers of unreinforced PPE materials. Certification validates that the poly(phenylene ether) materials meet globally recognized specifications for mechanical, thermal, and physical performance. It ensures that your products align with international expectations for reliability and material classification in technical applications. Certification Process for ISO 8986 Application Review – Evaluation of PPE material types, grades, and usage scope. Stage 1 Audit – Review of testing data, quality assurance protocols, and technical documentation. Stage 2 Audit – On-site verification of processing methods, material identification, and test equipment. Certification Decision – Issuance of ISO 8986-1:2020 certificate after successful audit and compliance confirmation. Surveillance Audits – Yearly evaluations to maintain ongoing conformity and material performance consistency. Recertification – Complete reassessment every three years to ensure continued certification. Benefits of ISO 8986 Certification Ensures standardized quality and classification of PPE materials. Supports product development in high-performance plastic applications. Improves customer trust and acceptance in regulated markets. Reduces variability in material performance across production batches. Promotes transparency and traceability in material selection. Demonstrates compliance with international material testing standards. Get ISO 8986 Certified with Us If your organization produces or supplies unreinforced PPE materials for moulding and extrusion, ISO 8986-1:2020 certification confirms material compliance and quality consistency. Quality Asia Certification offers reliable ISO certification services to help your products meet international market standards. Contact us today to begin your ISO 8986 certification process.

    Type of Certification : ISO 8986

    Industry Focus : Diverse

    Certification Body Accreditation : NABCB

    Implementation Timeline : 20 days

    Cost : Based On Company Size & Complexity

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  • ISO 8536 Certification Service

    ISO 8536 Certification Service

    25,000 / Set

    • Type of CertificationISO 8536
    • Industry FocusDiverse
    • Certification Body AccreditationNABCB
    • Implementation Timeline20 days
    • CostBased On Company Size & Complexity
    • ISO 8536:2019 Certification – Infusion Equipment for Medical Use Overview ISO 8536:2019 is an internationally recognized standard that specifies the requirements for infusion equipment used with pressure infusion apparatus and gravity-feed infusion systems. This standard plays a vital role in the medical and healthcare sector by ensuring the safety, quality, and compatibility of infusion devices. It helps manufacturers and suppliers maintain global conformity, reduce risks, and enhance patient safety during intravenous therapy. What is ISO 8536:2019? ISO 8536:2019 is a multipart standard titled "Infusion equipment for medical use ", developed by the International Organization for Standardization. It outlines performance and testing requirements for disposable infusion sets and accessories such as infusion containers, infusion sets for single use, burette infusion sets, injection sites, filters, pressure infusion devices, and related apparatus used in the delivery of fluids or drugs into a patient 's bloodstream. This version replaces earlier versions by refining testing methods and including safety updates based on technological advancements and clinical usage. The multipart nature of ISO 8536 ensures comprehensive coverage of various infusion-related devices and components. Why ISO 8536:2019 Certification? Obtaining ISO 8536:2019 certification assures that your medical infusion products comply with international quality and safety benchmarks. This certification demonstrates your commitment to delivering safe and reliable equipment for clinical use. It is particularly critical for manufacturers exporting medical devices or supplying hospitals, clinics, and healthcare institutions globally. Benefits of ISO 8536:2019 Certification Ensures Product Safety and Performance: Verifies that infusion equipment is designed and tested for safe usage under defined conditions. Regulatory Compliance: Helps meet national and international regulatory requirements in the healthcare and medical device sectors. Improved Market Access: Facilitates easier entry into global markets by aligning with internationally accepted standards. Reduced Risk of Failure: Minimizes the possibility of equipment malfunction, which can lead to adverse patient outcomes. Quality Assurance: Strengthens internal quality control processes, improving manufacturing consistency. Customer Trust: Enhances confidence among hospitals, clinics, and medical professionals using your products. Certification Process Application Submission: Provide product details and scope for which ISO 8536:2019 certification is required. Documentation Review: Verification of technical files, design specifications, and test results as per ISO 8536 parts. Product Evaluation: Physical inspection and sampling of infusion equipment based on standard testing protocols. Audit and Compliance Check: Assessment of production practices and risk management related to product manufacturing. Issuance of Certificate: On successful verification, the ISO 8536:2019 certificate is issued, valid for a specified period with surveillance audits. Benefit to Business Establishes a reputation as a reliable medical device manufacturer. Increases acceptance in government and private healthcare procurement. Demonstrates adherence to global safety and hygiene norms. Reduces product recalls and liability risks. Enhances competitiveness in both domestic and international markets. Supports continuous improvement through standardized testing and quality metrics
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  • ISO 8536 Certification Service

    ISO 8536 Certification Service

    25,000 / Set

    ISO 8536:2019 Certification – Infusion Equipment for Medical Use Overview ISO 8536:2019 is an internationally recognized standard that specifies the requirements for infusion equipment used with pressure infusion apparatus and gravity-feed infusion systems. This standard plays a vital role in the medical and healthcare sector by ensuring the safety, quality, and compatibility of infusion devices. It helps manufacturers and suppliers maintain global conformity, reduce risks, and enhance patient safety during intravenous therapy. What is ISO 8536:2019? ISO 8536:2019 is a multipart standard titled "Infusion equipment for medical use ", developed by the International Organization for Standardization. It outlines performance and testing requirements for disposable infusion sets and accessories such as infusion containers, infusion sets for single use, burette infusion sets, injection sites, filters, pressure infusion devices, and related apparatus used in the delivery of fluids or drugs into a patient 's bloodstream. This version replaces earlier versions by refining testing methods and including safety updates based on technological advancements and clinical usage. The multipart nature of ISO 8536 ensures comprehensive coverage of various infusion-related devices and components. Why ISO 8536:2019 Certification? Obtaining ISO 8536:2019 certification assures that your medical infusion products comply with international quality and safety benchmarks. This certification demonstrates your commitment to delivering safe and reliable equipment for clinical use. It is particularly critical for manufacturers exporting medical devices or supplying hospitals, clinics, and healthcare institutions globally. Benefits of ISO 8536:2019 Certification Ensures Product Safety and Performance: Verifies that infusion equipment is designed and tested for safe usage under defined conditions. Regulatory Compliance: Helps meet national and international regulatory requirements in the healthcare and medical device sectors. Improved Market Access: Facilitates easier entry into global markets by aligning with internationally accepted standards. Reduced Risk of Failure: Minimizes the possibility of equipment malfunction, which can lead to adverse patient outcomes. Quality Assurance: Strengthens internal quality control processes, improving manufacturing consistency. Customer Trust: Enhances confidence among hospitals, clinics, and medical professionals using your products. Certification Process Application Submission: Provide product details and scope for which ISO 8536:2019 certification is required. Documentation Review: Verification of technical files, design specifications, and test results as per ISO 8536 parts. Product Evaluation: Physical inspection and sampling of infusion equipment based on standard testing protocols. Audit and Compliance Check: Assessment of production practices and risk management related to product manufacturing. Issuance of Certificate: On successful verification, the ISO 8536:2019 certificate is issued, valid for a specified period with surveillance audits. Benefit to Business Establishes a reputation as a reliable medical device manufacturer. Increases acceptance in government and private healthcare procurement. Demonstrates adherence to global safety and hygiene norms. Reduces product recalls and liability risks. Enhances competitiveness in both domestic and international markets. Supports continuous improvement through standardized testing and quality metrics

    Type of Certification : ISO 8536

    Industry Focus : Diverse

    Certification Body Accreditation : NABCB

    Implementation Timeline : 20 days

    Cost : Based On Company Size & Complexity

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  • ISO 811 Certification Service

    ISO 811 Certification Service

    25,000 / Set

    • Type of CertificationISO 811
    • Industry FocusDiverse
    • Certification Body AccreditationNABCB
    • Implementation Timeline20 days
    • CostBased On Company Size & Complexity
    • What is ISO 811:2018? ISO 811:2018 is an internationally recognized testing standard that specifies a method for determining the resistance of textile fabrics to water penetration under hydrostatic pressure. Commonly known as the Hydrostatic Head Test, this method is used to evaluate the waterproof properties of coated and uncoated fabrics. The test measures how much water pressure a fabric can withstand before leakage occurs, making ISO 811 essential for industries dealing with waterproof clothing, tents, tarpaulins, medical textiles, and technical fabrics. ISO 811 – Overview ISO 811:2018 applies to textiles intended to resist water under pressure, such as rainwear, outdoor gear, and protective equipment. The method involves applying water at a constant rate of pressure to a fabric sample until water penetrates the surface. The result is recorded in millimeters of water column, which reflects the fabric 's waterproof capability. This standardized test ensures quality, consistency, and reliability of textile products across global markets. Compliance with ISO 811 is a sign of durability and functionality for end-use in demanding environmental conditions. ISO 811:2018 Testing Requirements Select a representative fabric sample for testing under standard atmospheric conditions. Place the fabric in a hydrostatic head testing apparatus as per ISO 811 guidelines. Apply water pressure gradually at a defined rate until water droplets appear on the fabric’s upper surface. Record the pressure level at the first sign of penetration, measured in mm H₂O. Repeat the test on multiple samples to ensure result consistency and reliability. Evaluate average performance to determine product waterproof rating. ISO 811 Applications and Use Cases Widely used by textile manufacturers, quality control labs, and product testing facilities. Essential for rainwear, military uniforms, outdoor gear, luggage fabrics, and industrial textiles. Relevant for hospital-grade products like mattress protectors, PPE garments, and cleanroom covers. Supports R&D and product innovation in fabric engineering and coating technologies. Benefits of ISO 811:2018 Compliance Assures end-users of product performance in wet conditions. Improves market acceptance by meeting international waterproofing standards. Reduces product recalls or complaints due to leakage or failure in water resistance. Enhances credibility and product trust for manufacturers and brands. Supports exports and tenders requiring standardized test certification. Why Choose Quality Asia Certification for ISO 811 At Quality Asia Certification, we offer ISO 811:2018 testing certification services that validate your fabric’s waterproof resistance using calibrated equipment and global best practices. Our certification provides credible proof that your products meet international hydrostatic pressure resistance benchmarks. With fast processing, clear reports, and global recognition, we help you showcase product quality and boost confidence in competitive markets.   Get Your Products Tested for ISO 811 Whether you manufacture outdoor textiles, medical fabric, or waterproof gear, ISO 811 certification can add value to your products. Partner with Quality Asia Certification to demonstrate compliance with international waterproofing standards and give your customers the assurance they demand.
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  • ISO 811 Certification Service

    ISO 811 Certification Service

    25,000 / Set

    What is ISO 811:2018? ISO 811:2018 is an internationally recognized testing standard that specifies a method for determining the resistance of textile fabrics to water penetration under hydrostatic pressure. Commonly known as the Hydrostatic Head Test, this method is used to evaluate the waterproof properties of coated and uncoated fabrics. The test measures how much water pressure a fabric can withstand before leakage occurs, making ISO 811 essential for industries dealing with waterproof clothing, tents, tarpaulins, medical textiles, and technical fabrics. ISO 811 – Overview ISO 811:2018 applies to textiles intended to resist water under pressure, such as rainwear, outdoor gear, and protective equipment. The method involves applying water at a constant rate of pressure to a fabric sample until water penetrates the surface. The result is recorded in millimeters of water column, which reflects the fabric 's waterproof capability. This standardized test ensures quality, consistency, and reliability of textile products across global markets. Compliance with ISO 811 is a sign of durability and functionality for end-use in demanding environmental conditions. ISO 811:2018 Testing Requirements Select a representative fabric sample for testing under standard atmospheric conditions. Place the fabric in a hydrostatic head testing apparatus as per ISO 811 guidelines. Apply water pressure gradually at a defined rate until water droplets appear on the fabric’s upper surface. Record the pressure level at the first sign of penetration, measured in mm H₂O. Repeat the test on multiple samples to ensure result consistency and reliability. Evaluate average performance to determine product waterproof rating. ISO 811 Applications and Use Cases Widely used by textile manufacturers, quality control labs, and product testing facilities. Essential for rainwear, military uniforms, outdoor gear, luggage fabrics, and industrial textiles. Relevant for hospital-grade products like mattress protectors, PPE garments, and cleanroom covers. Supports R&D and product innovation in fabric engineering and coating technologies. Benefits of ISO 811:2018 Compliance Assures end-users of product performance in wet conditions. Improves market acceptance by meeting international waterproofing standards. Reduces product recalls or complaints due to leakage or failure in water resistance. Enhances credibility and product trust for manufacturers and brands. Supports exports and tenders requiring standardized test certification. Why Choose Quality Asia Certification for ISO 811 At Quality Asia Certification, we offer ISO 811:2018 testing certification services that validate your fabric’s waterproof resistance using calibrated equipment and global best practices. Our certification provides credible proof that your products meet international hydrostatic pressure resistance benchmarks. With fast processing, clear reports, and global recognition, we help you showcase product quality and boost confidence in competitive markets.   Get Your Products Tested for ISO 811 Whether you manufacture outdoor textiles, medical fabric, or waterproof gear, ISO 811 certification can add value to your products. Partner with Quality Asia Certification to demonstrate compliance with international waterproofing standards and give your customers the assurance they demand.

    Type of Certification : ISO 811

    Industry Focus : Diverse

    Certification Body Accreditation : NABCB

    Implementation Timeline : 20 days

    Cost : Based On Company Size & Complexity

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  • ISO 8101 Certification Service

    ISO 8101 Certification Service

    25,000 / Sets

    • Type of CertificationISO 8101
    • Industry FocusDiverse
    • Certification Body AccreditationNABCB
    • Implementation Timeline20 days
    • CostBased On Company Size & Complexity
    • ISO 8101:2023 Certification – Human Resource Management Vocabulary Overview ISO 8101:2023 is an internationally recognized standard that defines a common vocabulary for human resource management (HRM). Developed by the International Organization for Standardization, this standard aims to harmonize terminology across HR functions to enhance clarity, communication, and consistency within and between organizations. It serves as a foundational reference for HR processes, enabling organizations to align their internal practices with globally accepted HR definitions. What is ISO 8101:2023? ISO 8101:2023 is part of the ISO 30400 family, which focuses on human resource management standards. Specifically, ISO 8101:2023 offers a comprehensive set of definitions and descriptions of terms used in various HRM domains such as recruitment, performance management, employee development, and workforce planning. The standard ensures that all stakeholders—whether HR professionals, management, employees, or external partners—understand and interpret HR-related terms uniformly. This reduces ambiguity and enhances the quality of HR data, reporting, and policy implementation. Why ISO 8101:2023? Standardized HR terminology is essential in today’s globally connected business environment. ISO 8101:2023 is particularly valuable for multinational companies, organizations with remote or cross-functional teams, and institutions seeking to improve internal HR processes or meet international compliance requirements. Misunderstanding of HR terms can lead to inefficiencies, compliance issues, or employee dissatisfaction. By using ISO 8101:2023, organizations gain a consistent and structured language that improves operational efficiency, communication, and employee relations. Benefits of ISO 8101:2023 Certification   Standardized Communication: Establishes a unified HR vocabulary that enhances internal communication and reduces misinterpretation of key HR concepts. Process Alignment: Aligns all HR activities and documentation to internationally accepted definitions, leading to improved quality and traceability. Global Compatibility: Facilitates smooth HR operations across international borders by harmonizing HR language with global practices. Support for Automation: Helps in the effective implementation of HR information systems (HRIS) and automation by standardizing data inputs. Regulatory Compliance: Assists in meeting legal and regulatory requirements where standardized HR documentation and definitions are required.
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  • ISO 8101 Certification Service

    ISO 8101 Certification Service

    25,000 / Sets

    ISO 8101:2023 Certification – Human Resource Management Vocabulary Overview ISO 8101:2023 is an internationally recognized standard that defines a common vocabulary for human resource management (HRM). Developed by the International Organization for Standardization, this standard aims to harmonize terminology across HR functions to enhance clarity, communication, and consistency within and between organizations. It serves as a foundational reference for HR processes, enabling organizations to align their internal practices with globally accepted HR definitions. What is ISO 8101:2023? ISO 8101:2023 is part of the ISO 30400 family, which focuses on human resource management standards. Specifically, ISO 8101:2023 offers a comprehensive set of definitions and descriptions of terms used in various HRM domains such as recruitment, performance management, employee development, and workforce planning. The standard ensures that all stakeholders—whether HR professionals, management, employees, or external partners—understand and interpret HR-related terms uniformly. This reduces ambiguity and enhances the quality of HR data, reporting, and policy implementation. Why ISO 8101:2023? Standardized HR terminology is essential in today’s globally connected business environment. ISO 8101:2023 is particularly valuable for multinational companies, organizations with remote or cross-functional teams, and institutions seeking to improve internal HR processes or meet international compliance requirements. Misunderstanding of HR terms can lead to inefficiencies, compliance issues, or employee dissatisfaction. By using ISO 8101:2023, organizations gain a consistent and structured language that improves operational efficiency, communication, and employee relations. Benefits of ISO 8101:2023 Certification   Standardized Communication: Establishes a unified HR vocabulary that enhances internal communication and reduces misinterpretation of key HR concepts. Process Alignment: Aligns all HR activities and documentation to internationally accepted definitions, leading to improved quality and traceability. Global Compatibility: Facilitates smooth HR operations across international borders by harmonizing HR language with global practices. Support for Automation: Helps in the effective implementation of HR information systems (HRIS) and automation by standardizing data inputs. Regulatory Compliance: Assists in meeting legal and regulatory requirements where standardized HR documentation and definitions are required.

    Type of Certification : ISO 8101

    Industry Focus : Diverse

    Certification Body Accreditation : NABCB

    Implementation Timeline : 20 days

    Cost : Based On Company Size & Complexity

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  • ISO 80001 Certification Service

    ISO 80001 Certification Service

    25,000 / Set

    • Type of CertificationISO 80001
    • Industry FocusDiverse
    • Certification Body AccreditationNABCB
    • Implementation Timeline20 days
    • CostBased On Company Size & Complexity
    • What is ISO 80001-1:2021? ISO 80001-1:2021 is an international standard that provides guidance for the application of risk management to IT networks that incorporate medical devices. It is particularly relevant for healthcare providers, hospitals, and medical device manufacturers aiming to ensure the safety, effectiveness, and security of networked medical systems. The standard helps organizations manage risks related to the integration of medical devices with IT infrastructure, ensuring patient safety and operational continuity. ISO 80001 – Overview With the increasing use of connected medical devices and digital health systems, the integration of IT and healthcare technologies poses significant safety and cybersecurity challenges. ISO 80001-1:2021 offers a structured approach to identifying, assessing, and controlling risks in these environments. It emphasizes the responsibility of healthcare delivery organizations to ensure the safe use of medical IT networks. The standard supports compliance with regulatory frameworks while promoting effective communication between stakeholders such as IT professionals, clinical engineers, and medical staff. ISO 80001-1:2021 Key Requirements Establish clear responsibilities for the safe integration of medical devices into IT networks. Identify and evaluate potential risks that could impact safety, effectiveness, or data integrity. Apply a risk management process that includes risk identification, analysis, evaluation, control, and monitoring. Ensure traceability of risk-related decisions and maintain detailed documentation. Promote collaboration among IT, clinical, and biomedical teams to manage medical IT networks. Implement procedures to detect and respond to cybersecurity threats or device malfunctions. Maintain device functionality and data integrity during software updates or network changes. Ensure that medical device manufacturers provide necessary risk-related information to healthcare organizations. ISO 80001-1:2021 Implementation Support Quality Asia Certification offers certification services to organizations aiming to adopt ISO 80001-1:2021 for enhanced risk management of their medical IT networks. Certification demonstrates a proactive approach to managing technological risks in healthcare environments and helps build trust among patients, regulators, and technology partners. Organizations seeking ISO 80001 certification must implement a comprehensive risk management framework that aligns with the standard’s principles and ensures safety and reliability in interconnected systems. ISO 80001-1:2021 Certification Process Initial Assessment – Review of existing IT and medical device network setup and risk management practices. Risk Management Framework – Verification of structured procedures to identify and control network-related risks. Documentation Review – Evaluation of risk logs, safety protocols, responsibilities, and device integration plans. On-Site Audit – Examination of implemented controls, network operations, and safety assurance procedures. Certification Decision – Issuance of ISO 80001-1:2021 certificate upon successful audit and compliance verification.   Get Certified with ISO 80001-1:2021 If your organization is involved in operating or managing medical IT networks, ISO 80001-1:2021 certification can demonstrate your commitment to risk management, patient safety, and data security. Quality Asia Certification provides robust and recognized certification services that validate your compliance with international standards. Achieve ISO 80001 certification to enhance system reliability, meet healthcare regulations, and strengthen stakeholder confidence.
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  • ISO 80001 Certification Service

    ISO 80001 Certification Service

    25,000 / Set

    What is ISO 80001-1:2021? ISO 80001-1:2021 is an international standard that provides guidance for the application of risk management to IT networks that incorporate medical devices. It is particularly relevant for healthcare providers, hospitals, and medical device manufacturers aiming to ensure the safety, effectiveness, and security of networked medical systems. The standard helps organizations manage risks related to the integration of medical devices with IT infrastructure, ensuring patient safety and operational continuity. ISO 80001 – Overview With the increasing use of connected medical devices and digital health systems, the integration of IT and healthcare technologies poses significant safety and cybersecurity challenges. ISO 80001-1:2021 offers a structured approach to identifying, assessing, and controlling risks in these environments. It emphasizes the responsibility of healthcare delivery organizations to ensure the safe use of medical IT networks. The standard supports compliance with regulatory frameworks while promoting effective communication between stakeholders such as IT professionals, clinical engineers, and medical staff. ISO 80001-1:2021 Key Requirements Establish clear responsibilities for the safe integration of medical devices into IT networks. Identify and evaluate potential risks that could impact safety, effectiveness, or data integrity. Apply a risk management process that includes risk identification, analysis, evaluation, control, and monitoring. Ensure traceability of risk-related decisions and maintain detailed documentation. Promote collaboration among IT, clinical, and biomedical teams to manage medical IT networks. Implement procedures to detect and respond to cybersecurity threats or device malfunctions. Maintain device functionality and data integrity during software updates or network changes. Ensure that medical device manufacturers provide necessary risk-related information to healthcare organizations. ISO 80001-1:2021 Implementation Support Quality Asia Certification offers certification services to organizations aiming to adopt ISO 80001-1:2021 for enhanced risk management of their medical IT networks. Certification demonstrates a proactive approach to managing technological risks in healthcare environments and helps build trust among patients, regulators, and technology partners. Organizations seeking ISO 80001 certification must implement a comprehensive risk management framework that aligns with the standard’s principles and ensures safety and reliability in interconnected systems. ISO 80001-1:2021 Certification Process Initial Assessment – Review of existing IT and medical device network setup and risk management practices. Risk Management Framework – Verification of structured procedures to identify and control network-related risks. Documentation Review – Evaluation of risk logs, safety protocols, responsibilities, and device integration plans. On-Site Audit – Examination of implemented controls, network operations, and safety assurance procedures. Certification Decision – Issuance of ISO 80001-1:2021 certificate upon successful audit and compliance verification.   Get Certified with ISO 80001-1:2021 If your organization is involved in operating or managing medical IT networks, ISO 80001-1:2021 certification can demonstrate your commitment to risk management, patient safety, and data security. Quality Asia Certification provides robust and recognized certification services that validate your compliance with international standards. Achieve ISO 80001 certification to enhance system reliability, meet healthcare regulations, and strengthen stakeholder confidence.

    Type of Certification : ISO 80001

    Industry Focus : Diverse

    Certification Body Accreditation : NABCB

    Implementation Timeline : 20 days

    Cost : Based On Company Size & Complexity

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  • ISO 7101 Certification Service

    ISO 7101 Certification Service

    25,000 / Set

    • Type of CertificationISO 7101
    • Industry FocusDiverse
    • Certification Body AccreditationNABCB
    • Implementation Timeline20 days
    • CostBased On Company Size & Complexity
    • ISO 7101:2023 Certification – Quality Asia Certification Overview ISO 7101:2023 is the international standard for healthcare quality management systems, titled “Health care organization management — Management systems for quality in health care organizations — Requirements.” This standard provides a framework to establish, implement, maintain, and improve a quality management system specifically designed for healthcare organizations. ISO 7101:2023 focuses on patient-centered care, risk management, stakeholder engagement, and continual improvement, helping healthcare institutions deliver safe, effective, and high-quality services. What is ISO 7101:2023? ISO 7101:2023 is designed for healthcare organizations of all sizes and types, including hospitals, clinics, diagnostic centers, and home care providers. It aligns with principles such as evidence-based decision-making, leadership commitment, competency development, and integrated management practices. The standard supports organizations in meeting regulatory and patient requirements while enhancing transparency, operational control, and clinical outcomes. It integrates seamlessly with other ISO management system standards such as ISO 9001. Why ISO 7101:2023 Certification? ISO 7101:2023 certification demonstrates an organization’s commitment to delivering high-quality healthcare services through an effective quality management system. In an industry where patient safety and service excellence are critical, this certification boosts confidence among patients, regulatory bodies, insurance providers, and other stakeholders. It acts as a strategic tool to reduce clinical errors, improve efficiency, and build trust. Requirements for ISO 7101:2023 Certification To achieve ISO 7101:2023 certification, a healthcare organization must: Define quality objectives aligned with patient and stakeholder needs Establish processes for clinical and operational risk management Ensure regulatory compliance and ethical practices Implement a structured framework for leadership, communication, and resource planning Monitor patient satisfaction and clinical outcomes Conduct internal audits and management reviews Promote staff competency, engagement, and continuous professional development Certification Process   Gap Analysis – Assess current systems against ISO 7101:2023 requirements System Development – Establish or update processes, controls, and documentation Implementation – Apply the system across all operational levels Internal Audit – Verify readiness and identify areas for improvement Management Review – Ensure top management involvement and decision-making Stage 1 Audit – Review documentation and process preparedness Stage 2 Audit – Evaluate implementation effectiveness across operations Certification Decision – Upon successful audit, ISO 7101:2023 certification is granted Surveillance Audits – Conducted annually to maintain certification validity
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  • ISO 7101 Certification Service

    ISO 7101 Certification Service

    25,000 / Set

    ISO 7101:2023 Certification – Quality Asia Certification Overview ISO 7101:2023 is the international standard for healthcare quality management systems, titled “Health care organization management — Management systems for quality in health care organizations — Requirements.” This standard provides a framework to establish, implement, maintain, and improve a quality management system specifically designed for healthcare organizations. ISO 7101:2023 focuses on patient-centered care, risk management, stakeholder engagement, and continual improvement, helping healthcare institutions deliver safe, effective, and high-quality services. What is ISO 7101:2023? ISO 7101:2023 is designed for healthcare organizations of all sizes and types, including hospitals, clinics, diagnostic centers, and home care providers. It aligns with principles such as evidence-based decision-making, leadership commitment, competency development, and integrated management practices. The standard supports organizations in meeting regulatory and patient requirements while enhancing transparency, operational control, and clinical outcomes. It integrates seamlessly with other ISO management system standards such as ISO 9001. Why ISO 7101:2023 Certification? ISO 7101:2023 certification demonstrates an organization’s commitment to delivering high-quality healthcare services through an effective quality management system. In an industry where patient safety and service excellence are critical, this certification boosts confidence among patients, regulatory bodies, insurance providers, and other stakeholders. It acts as a strategic tool to reduce clinical errors, improve efficiency, and build trust. Requirements for ISO 7101:2023 Certification To achieve ISO 7101:2023 certification, a healthcare organization must: Define quality objectives aligned with patient and stakeholder needs Establish processes for clinical and operational risk management Ensure regulatory compliance and ethical practices Implement a structured framework for leadership, communication, and resource planning Monitor patient satisfaction and clinical outcomes Conduct internal audits and management reviews Promote staff competency, engagement, and continuous professional development Certification Process   Gap Analysis – Assess current systems against ISO 7101:2023 requirements System Development – Establish or update processes, controls, and documentation Implementation – Apply the system across all operational levels Internal Audit – Verify readiness and identify areas for improvement Management Review – Ensure top management involvement and decision-making Stage 1 Audit – Review documentation and process preparedness Stage 2 Audit – Evaluate implementation effectiveness across operations Certification Decision – Upon successful audit, ISO 7101:2023 certification is granted Surveillance Audits – Conducted annually to maintain certification validity

    Type of Certification : ISO 7101

    Industry Focus : Diverse

    Certification Body Accreditation : NABCB

    Implementation Timeline : 20 days

    Cost : Based On Company Size & Complexity

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  • ISO 679 Certification Service

    ISO 679 Certification Service

    25,000 / Sets

    • Type of CertificationISO 679
    • Industry FocusDiverse
    • Certification Body AccreditationNABCB
    • Implementation Timeline20 days
    • CostBased On Company Size & Complexity
    • ISO 679:2023 Certification – Quality Asia Certification Overview ISO 679:2023 is an internationally recognized standard developed by the International Organization for Standardization (ISO) that specifies the method for determining the compressive strength of hydraulic cement mortars. It ensures that testing procedures for cement strength are accurate, repeatable, and aligned globally. The standard is crucial for quality control in the cement and construction industry, offering consistent benchmarks for evaluating performance and durability. What is ISO 679:2023? ISO 679:2023 titled “Cement — Test methods — Determination of strength” defines the standardized process for preparing and testing mortar specimens made from hydraulic cement to measure their compressive strength. The test results support compliance with industry-specific strength requirements and assist in identifying batch quality for both manufacturers and construction professionals. The standard is widely used by laboratories, construction firms, quality control departments, and regulatory agencies. Why ISO 679:2023? Hydraulic cement plays a central role in the strength and stability of concrete structures. Inconsistent testing methods can lead to inaccurate strength estimations, posing risks to safety and performance. ISO 679:2023 helps eliminate such variability by setting uniform procedures. Adopting this certification shows a commitment to material quality, operational excellence, and adherence to global standards in construction and manufacturing. Requirements for ISO 679:2023 Certification Organizations seeking ISO 679:2023 certification should be capable of: Preparing standard mortar samples as per the prescribed mix proportions and curing conditions Utilizing calibrated testing equipment for compressive strength measurements Maintaining a controlled laboratory environment for testing accuracy Recording and reporting data as per ISO 679 protocols Implementing internal quality procedures to ensure testing reliability and traceability Key documentation typically includes equipment calibration records, mortar composition data, environmental control logs, and test result reports. All procedures must align with the technical requirements detailed in ISO 679:2023. ISO 679:2023 Certification Process Application Submission – Share basic organization and testing facility details for preliminary review. Document Evaluation – Assess equipment calibration, sample preparation, and test result recording procedures. On-site Audit – Verify laboratory practices, personnel competence, and conformity to ISO 679:2023. Report & Review – A detailed report is prepared highlighting compliance and any non-conformities. Certification Issuance – Upon successful audit, the ISO 679:2023 certificate is issued with defined validity. Surveillance Audits – Periodic checks ensure ongoing compliance with the standard. Benefits of ISO 679:2023 Certification Ensures globally accepted testing methods for cement strength Boosts confidence in construction material performance Enhances credibility with clients, suppliers, and regulators Reduces risk of structural failure through standardized quality checks Supports research and development through consistent benchmarking Helps meet contractual and regulatory requirements in infrastructure projects Benefit to Business   Improved Quality Assurance: Demonstrates rigorous internal control over testing processes. Market Access: Facilitates acceptance in national and international construction markets. Risk Mitigation: Reduces liability through validated, repeatable testing methods. Operational Efficiency: Streamlines laboratory operations and documentation. Customer Trust: Builds stakeholder confidence in the accuracy of product performance data.
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  • ISO 679 Certification Service

    ISO 679 Certification Service

    25,000 / Sets

    ISO 679:2023 Certification – Quality Asia Certification Overview ISO 679:2023 is an internationally recognized standard developed by the International Organization for Standardization (ISO) that specifies the method for determining the compressive strength of hydraulic cement mortars. It ensures that testing procedures for cement strength are accurate, repeatable, and aligned globally. The standard is crucial for quality control in the cement and construction industry, offering consistent benchmarks for evaluating performance and durability. What is ISO 679:2023? ISO 679:2023 titled “Cement — Test methods — Determination of strength” defines the standardized process for preparing and testing mortar specimens made from hydraulic cement to measure their compressive strength. The test results support compliance with industry-specific strength requirements and assist in identifying batch quality for both manufacturers and construction professionals. The standard is widely used by laboratories, construction firms, quality control departments, and regulatory agencies. Why ISO 679:2023? Hydraulic cement plays a central role in the strength and stability of concrete structures. Inconsistent testing methods can lead to inaccurate strength estimations, posing risks to safety and performance. ISO 679:2023 helps eliminate such variability by setting uniform procedures. Adopting this certification shows a commitment to material quality, operational excellence, and adherence to global standards in construction and manufacturing. Requirements for ISO 679:2023 Certification Organizations seeking ISO 679:2023 certification should be capable of: Preparing standard mortar samples as per the prescribed mix proportions and curing conditions Utilizing calibrated testing equipment for compressive strength measurements Maintaining a controlled laboratory environment for testing accuracy Recording and reporting data as per ISO 679 protocols Implementing internal quality procedures to ensure testing reliability and traceability Key documentation typically includes equipment calibration records, mortar composition data, environmental control logs, and test result reports. All procedures must align with the technical requirements detailed in ISO 679:2023. ISO 679:2023 Certification Process Application Submission – Share basic organization and testing facility details for preliminary review. Document Evaluation – Assess equipment calibration, sample preparation, and test result recording procedures. On-site Audit – Verify laboratory practices, personnel competence, and conformity to ISO 679:2023. Report & Review – A detailed report is prepared highlighting compliance and any non-conformities. Certification Issuance – Upon successful audit, the ISO 679:2023 certificate is issued with defined validity. Surveillance Audits – Periodic checks ensure ongoing compliance with the standard. Benefits of ISO 679:2023 Certification Ensures globally accepted testing methods for cement strength Boosts confidence in construction material performance Enhances credibility with clients, suppliers, and regulators Reduces risk of structural failure through standardized quality checks Supports research and development through consistent benchmarking Helps meet contractual and regulatory requirements in infrastructure projects Benefit to Business   Improved Quality Assurance: Demonstrates rigorous internal control over testing processes. Market Access: Facilitates acceptance in national and international construction markets. Risk Mitigation: Reduces liability through validated, repeatable testing methods. Operational Efficiency: Streamlines laboratory operations and documentation. Customer Trust: Builds stakeholder confidence in the accuracy of product performance data.

    Type of Certification : ISO 679

    Industry Focus : Diverse

    Certification Body Accreditation : NABCB

    Implementation Timeline : 20 days

    Cost : Based On Company Size & Complexity

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  • ISO 50015 Certification Service

    ISO 50015 Certification Service

    25,000 / Set

    • Type of CertificationISO 50015
    • Industry FocusDiverse
    • Certification Body AccreditationNABCB
    • Implementation Timeline20 days
    • CostBased On Company Size & Complexity
    • Pre-Audit SupportAvailable
    • What is ISO 50015:2014? ISO 50015:2014 is an international standard that provides general principles and guidance for measuring and verifying energy performance in organizations. It supports the implementation of energy management systems by establishing methods to assess and demonstrate improvements in energy efficiency. The standard helps organizations validate energy savings resulting from energy performance improvement actions in a credible, consistent, and transparent manner. ISO 50015 – Overview ISO 50015 is designed to align with ISO 50001 and offers a structured approach to measurement and verification (M&V) of energy performance. It helps establish reliable data collection, analysis, and reporting procedures for evaluating energy-saving initiatives. Applicable across all industries and sectors, ISO 50015 ensures that energy-related data is accurate, traceable, and suitable for decision-making. It enhances confidence in reported energy savings, which is essential for management reviews, regulatory compliance, or internal assessments. ISO 50015:2014 Key Requirements Define measurement boundaries and establish baseline conditions. Select appropriate energy performance indicators (EnPIs). Document M&V plans tailored to specific energy improvement activities. Use consistent methods to gather and analyze energy data. Establish quality assurance procedures for measurement tools and data handling. Ensure traceability and reproducibility of reported energy results. Maintain transparent records and documentation to support verification. ISO 50015 Training and Implementation Support ISO 50015 emphasizes planning, implementation, and continual improvement of M&V processes. Organizations must train internal teams to understand key M&V concepts such as data normalization, uncertainty analysis, and performance baselining. Proper training ensures reliable data interpretation and consistent application of the standard across multiple projects or facilities. Aligning ISO 50015 with energy performance systems promotes long-term efficiency and resource optimization. ISO 50015 Certification Preparation Process Initial Assessment – Identify current energy monitoring practices and relevant EnPIs. M&V Plan Development – Define scope, methods, and responsibilities for energy measurement. Data Management – Implement systems for accurate, repeatable, and secure energy data collection. Performance Evaluation – Monitor energy-saving activities and assess actual results against baselines. Compliance Review – Prepare documentation and internal evaluations to demonstrate conformity with ISO 50015.   Contact Us for ISO 50015 Certification ISO 50015:2014 supports organizations in achieving verified energy performance improvements with measurable outcomes. At Quality Asia Certification, we offer globally recognized certification services for ISO 50015 to help organizations validate and demonstrate the success of their energy-saving efforts. Whether your goal is to enhance operational efficiency, meet compliance expectations, or reinforce your sustainability initiatives, ISO 50015 enables you to build credibility through accurate and standardized measurement practices. Connect with us to begin your ISO 50015 certification journey today.
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  • ISO 50015 Certification Service

    ISO 50015 Certification Service

    25,000 / Set

    What is ISO 50015:2014? ISO 50015:2014 is an international standard that provides general principles and guidance for measuring and verifying energy performance in organizations. It supports the implementation of energy management systems by establishing methods to assess and demonstrate improvements in energy efficiency. The standard helps organizations validate energy savings resulting from energy performance improvement actions in a credible, consistent, and transparent manner. ISO 50015 – Overview ISO 50015 is designed to align with ISO 50001 and offers a structured approach to measurement and verification (M&V) of energy performance. It helps establish reliable data collection, analysis, and reporting procedures for evaluating energy-saving initiatives. Applicable across all industries and sectors, ISO 50015 ensures that energy-related data is accurate, traceable, and suitable for decision-making. It enhances confidence in reported energy savings, which is essential for management reviews, regulatory compliance, or internal assessments. ISO 50015:2014 Key Requirements Define measurement boundaries and establish baseline conditions. Select appropriate energy performance indicators (EnPIs). Document M&V plans tailored to specific energy improvement activities. Use consistent methods to gather and analyze energy data. Establish quality assurance procedures for measurement tools and data handling. Ensure traceability and reproducibility of reported energy results. Maintain transparent records and documentation to support verification. ISO 50015 Training and Implementation Support ISO 50015 emphasizes planning, implementation, and continual improvement of M&V processes. Organizations must train internal teams to understand key M&V concepts such as data normalization, uncertainty analysis, and performance baselining. Proper training ensures reliable data interpretation and consistent application of the standard across multiple projects or facilities. Aligning ISO 50015 with energy performance systems promotes long-term efficiency and resource optimization. ISO 50015 Certification Preparation Process Initial Assessment – Identify current energy monitoring practices and relevant EnPIs. M&V Plan Development – Define scope, methods, and responsibilities for energy measurement. Data Management – Implement systems for accurate, repeatable, and secure energy data collection. Performance Evaluation – Monitor energy-saving activities and assess actual results against baselines. Compliance Review – Prepare documentation and internal evaluations to demonstrate conformity with ISO 50015.   Contact Us for ISO 50015 Certification ISO 50015:2014 supports organizations in achieving verified energy performance improvements with measurable outcomes. At Quality Asia Certification, we offer globally recognized certification services for ISO 50015 to help organizations validate and demonstrate the success of their energy-saving efforts. Whether your goal is to enhance operational efficiency, meet compliance expectations, or reinforce your sustainability initiatives, ISO 50015 enables you to build credibility through accurate and standardized measurement practices. Connect with us to begin your ISO 50015 certification journey today.

    Type of Certification : ISO 50015

    Industry Focus : Diverse

    Certification Body Accreditation : NABCB

    Implementation Timeline : 20 days

    Cost : Based On Company Size & Complexity

    Pre-Audit Support : Available

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  • ISO 50001 Certification Services

    ISO 50001 Certification Services

    25,000 / Number

    • Provider TypeAccredited Certification Body
    • Certification Audits (Stages)Stage 1 & Stage 2
    • Post-certification SupportIncluded
    • TypeISO 50001
    • What is ISO 50001:2018?ISO 50001:2018 is an international standard developed by the International Organization for Standardization (ISO) that provides a framework for establishing, implementing, maintaining, and improving an energy management system (EnMS). It is designed to help organizations improve energy performance, increase energy efficiency, and reduce energy consumption and greenhouse gas emissions. The standard is applicable to organizations of all sizes and sectors that seek to manage their energy systematically. ISO 50001 – OverviewISO 50001:2018 is based on the ISO High-Level Structure (HLS), making it compatible with other standards like ISO 9001 and ISO 14001. It promotes a data-driven approach to energy management and encourages continual improvement through structured planning, monitoring, and performance evaluation. The standard empowers organizations to integrate energy efficiency into daily operations, enhance operational control, and lower utility costs over time. By aligning energy management with business strategy, ISO 50001 supports both sustainability and profitability goals. ISO 50001:2018 Key RequirementsEstablish an energy policy that reflects the organization 's commitment to energy performance.Conduct an energy review to identify significant energy uses and improvement opportunities.Define energy performance indicators (EnPIs) and set measurable energy objectives and targets.Ensure energy data is regularly monitored, measured, and analyzed for continual improvement.Incorporate energy-efficient design and procurement practices.Provide training and awareness to employees about their roles in energy management.Conduct internal audits and management reviews to evaluate system performance.Maintain documented information to demonstrate compliance with ISO 50001 requirements. Implementation and Benefits of ISO 50001:2018Organizations implementing ISO 50001:2018 benefit from improved control over energy use and operational costs. It encourages proactive energy-saving initiatives, leading to long-term cost reductions and enhanced competitiveness. Implementation also helps meet regulatory obligations, demonstrate environmental responsibility, and improve stakeholder confidence. The standard supports climate action by helping reduce carbon emissions and promoting a culture of sustainability. It also enhances equipment efficiency, optimizes energy-intensive processes, and reduces reliance on non-renewable energy sources. ISO 50001:2018 Certification ProcessApplication and Scope Definition – Identify applicable sites, energy sources, and boundaries of the EnMS.Stage 1 Audit – Evaluate documentation, readiness, and understanding of ISO 50001 requirements.Stage 2 Audit – Assess implementation and effectiveness of the energy management system in practice.Non-Conformity Closure – Address any findings and submit corrective actions.Certification Decision – Upon successful audit completion, ISO 50001:2018 certification is granted.Surveillance Audits – Conducted annually to ensure continued compliance and performance.Recertification – Performed every three years to maintain the validity of the certificate. Get ISO 50001 Certified with Quality Asia CertificationIf your organization is committed to improving energy efficiency and reducing its environmental impact, ISO 50001:2018 certification is the right step. Quality Asia Certification provides certification services to help your business demonstrate compliance with international energy management standards. Achieve recognition for your energy-saving efforts, enhance your brand value, and drive continual improvement through globally accepted best practices. Contact us to begin your ISO 50001 certification process and take a lead in responsible energy management.
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  • ISO 50001 Certification Services

    ISO 50001 Certification Services

    25,000 / Number

    What is ISO 50001:2018?ISO 50001:2018 is an international standard developed by the International Organization for Standardization (ISO) that provides a framework for establishing, implementing, maintaining, and improving an energy management system (EnMS). It is designed to help organizations improve energy performance, increase energy efficiency, and reduce energy consumption and greenhouse gas emissions. The standard is applicable to organizations of all sizes and sectors that seek to manage their energy systematically. ISO 50001 – OverviewISO 50001:2018 is based on the ISO High-Level Structure (HLS), making it compatible with other standards like ISO 9001 and ISO 14001. It promotes a data-driven approach to energy management and encourages continual improvement through structured planning, monitoring, and performance evaluation. The standard empowers organizations to integrate energy efficiency into daily operations, enhance operational control, and lower utility costs over time. By aligning energy management with business strategy, ISO 50001 supports both sustainability and profitability goals. ISO 50001:2018 Key RequirementsEstablish an energy policy that reflects the organization 's commitment to energy performance.Conduct an energy review to identify significant energy uses and improvement opportunities.Define energy performance indicators (EnPIs) and set measurable energy objectives and targets.Ensure energy data is regularly monitored, measured, and analyzed for continual improvement.Incorporate energy-efficient design and procurement practices.Provide training and awareness to employees about their roles in energy management.Conduct internal audits and management reviews to evaluate system performance.Maintain documented information to demonstrate compliance with ISO 50001 requirements. Implementation and Benefits of ISO 50001:2018Organizations implementing ISO 50001:2018 benefit from improved control over energy use and operational costs. It encourages proactive energy-saving initiatives, leading to long-term cost reductions and enhanced competitiveness. Implementation also helps meet regulatory obligations, demonstrate environmental responsibility, and improve stakeholder confidence. The standard supports climate action by helping reduce carbon emissions and promoting a culture of sustainability. It also enhances equipment efficiency, optimizes energy-intensive processes, and reduces reliance on non-renewable energy sources. ISO 50001:2018 Certification ProcessApplication and Scope Definition – Identify applicable sites, energy sources, and boundaries of the EnMS.Stage 1 Audit – Evaluate documentation, readiness, and understanding of ISO 50001 requirements.Stage 2 Audit – Assess implementation and effectiveness of the energy management system in practice.Non-Conformity Closure – Address any findings and submit corrective actions.Certification Decision – Upon successful audit completion, ISO 50001:2018 certification is granted.Surveillance Audits – Conducted annually to ensure continued compliance and performance.Recertification – Performed every three years to maintain the validity of the certificate. Get ISO 50001 Certified with Quality Asia CertificationIf your organization is committed to improving energy efficiency and reducing its environmental impact, ISO 50001:2018 certification is the right step. Quality Asia Certification provides certification services to help your business demonstrate compliance with international energy management standards. Achieve recognition for your energy-saving efforts, enhance your brand value, and drive continual improvement through globally accepted best practices. Contact us to begin your ISO 50001 certification process and take a lead in responsible energy management.

    Provider Type : Accredited Certification Body

    Certification Audits (Stages) : Stage 1 & Stage 2

    Post-certification Support : Included

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  • ISO 4992 Certification Service

    ISO 4992 Certification Service

    25,000 / number

    • Type of CertificationISO 4992
    • Industry FocusDiverse
    • Certification Body AccreditationNABCB
    • Implementation Timeline20 days
    • CostBased On Company Size & Complexity
    • ISO 4992:2020 Certification – Overview, Requirements, Certification Process, and Benefits Overview: ISO 4992:2020 specifies the acceptance levels for steel castings determined by ultrasonic testing. It is divided into two parts: ISO 4992-1:2020 – Steel castings for general purposes. ISO 4992-2:2020 – Steel castings for highly stressed components. This standard is vital for industries that require quality assurance in cast components where internal discontinuities may affect structural performance. ISO 4992 ensures that ultrasonic testing procedures are uniformly applied to detect internal flaws, promoting safety, consistency, and reliability in production. What is ISO 4992:2020? ISO 4992:2020 is an international standard developed by the International Organization for Standardization (ISO) focusing on non-destructive testing (NDT) using ultrasonic methods for evaluating steel castings. The two-part standard helps classify acceptance levels based on the severity of internal discontinuities. Part 1 (General purposes) outlines acceptance criteria for typical industrial applications. Part 2 (Highly stressed components) applies stricter controls for parts used in critical applications like aerospace, pressure vessels, or heavy machinery. Why ISO 4992:2020 Certification? Organizations opt for ISO 4992:2020 certification to demonstrate their commitment to producing quality steel castings with reliable internal integrity. This standard is especially crucial in sectors where structural failure can lead to significant operational and safety risks. Certification ensures customer confidence, compliance with industry best practices, and alignment with global quality expectations. Requirements for ISO 4992:2020 Certification: To prepare for ISO 4992:2020 certification, organizations must implement the following: Maintain documented ultrasonic testing procedures aligned with ISO 4992-1 or ISO 4992-2. Define acceptance levels (e.g., severity classes) suitable for the end-use application. Ensure availability of calibrated ultrasonic equipment and trained personnel. Keep inspection records that trace back to specific casting batches. Conduct internal audits and review results for conformance. Ensure corrective actions and traceability systems are in place. Certification Process: Gap Assessment: Review current ultrasonic testing practices against ISO 4992:2020 requirements. Documentation Review: Verify written procedures, acceptance criteria, and test records. On-site Audit: A third-party auditor evaluates ultrasonic testing practices, personnel competence, equipment, and inspection outcomes. Non-conformity Closure: Address any deviations found during the audit. Issuance of Certificate: Upon successful audit, the ISO 4992:2020 certificate is awarded, demonstrating compliance. Surveillance Audits: Annual checks are conducted to ensure ongoing conformity. Benefits of ISO 4992:2020 Certification:   Improved product reliability: Ensures steel castings meet internal quality expectations. Enhanced safety: Reduces the risk of failure in critical applications. Market recognition: Builds trust with clients and partners in engineering and manufacturing sectors. Regulatory compliance: Supports compliance with national and international technical specifications. Reduced rework and waste: Early defect detection through ultrasonic testing reduces scrap costs. Competitive advantage: Certification acts as proof of technical capability in NDT practices.
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  • ISO 4992 Certification Service

    ISO 4992 Certification Service

    25,000 / number

    ISO 4992:2020 Certification – Overview, Requirements, Certification Process, and Benefits Overview: ISO 4992:2020 specifies the acceptance levels for steel castings determined by ultrasonic testing. It is divided into two parts: ISO 4992-1:2020 – Steel castings for general purposes. ISO 4992-2:2020 – Steel castings for highly stressed components. This standard is vital for industries that require quality assurance in cast components where internal discontinuities may affect structural performance. ISO 4992 ensures that ultrasonic testing procedures are uniformly applied to detect internal flaws, promoting safety, consistency, and reliability in production. What is ISO 4992:2020? ISO 4992:2020 is an international standard developed by the International Organization for Standardization (ISO) focusing on non-destructive testing (NDT) using ultrasonic methods for evaluating steel castings. The two-part standard helps classify acceptance levels based on the severity of internal discontinuities. Part 1 (General purposes) outlines acceptance criteria for typical industrial applications. Part 2 (Highly stressed components) applies stricter controls for parts used in critical applications like aerospace, pressure vessels, or heavy machinery. Why ISO 4992:2020 Certification? Organizations opt for ISO 4992:2020 certification to demonstrate their commitment to producing quality steel castings with reliable internal integrity. This standard is especially crucial in sectors where structural failure can lead to significant operational and safety risks. Certification ensures customer confidence, compliance with industry best practices, and alignment with global quality expectations. Requirements for ISO 4992:2020 Certification: To prepare for ISO 4992:2020 certification, organizations must implement the following: Maintain documented ultrasonic testing procedures aligned with ISO 4992-1 or ISO 4992-2. Define acceptance levels (e.g., severity classes) suitable for the end-use application. Ensure availability of calibrated ultrasonic equipment and trained personnel. Keep inspection records that trace back to specific casting batches. Conduct internal audits and review results for conformance. Ensure corrective actions and traceability systems are in place. Certification Process: Gap Assessment: Review current ultrasonic testing practices against ISO 4992:2020 requirements. Documentation Review: Verify written procedures, acceptance criteria, and test records. On-site Audit: A third-party auditor evaluates ultrasonic testing practices, personnel competence, equipment, and inspection outcomes. Non-conformity Closure: Address any deviations found during the audit. Issuance of Certificate: Upon successful audit, the ISO 4992:2020 certificate is awarded, demonstrating compliance. Surveillance Audits: Annual checks are conducted to ensure ongoing conformity. Benefits of ISO 4992:2020 Certification:   Improved product reliability: Ensures steel castings meet internal quality expectations. Enhanced safety: Reduces the risk of failure in critical applications. Market recognition: Builds trust with clients and partners in engineering and manufacturing sectors. Regulatory compliance: Supports compliance with national and international technical specifications. Reduced rework and waste: Early defect detection through ultrasonic testing reduces scrap costs. Competitive advantage: Certification acts as proof of technical capability in NDT practices.

    Type of Certification : ISO 4992

    Industry Focus : Diverse

    Certification Body Accreditation : NABCB

    Implementation Timeline : 20 days

    Cost : Based On Company Size & Complexity

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  • ISO 4952 Certification Service

    ISO 4952 Certification Service

    25,000 / Set

    • Type of CertificationISO 4952
    • Industry FocusDiverse
    • Certification Body AccreditationNABCB
    • Implementation Timeline20 days
    • CostBased On Company Size & Complexity
    • What is ISO 4952:2020? ISO 4952:2020 is an international standard that specifies the requirements for hot-rolled nickel-chromium-based corrosion-resistant alloy plate, sheet, and strip. These materials are commonly used in applications requiring high resistance to corrosion, oxidation, and heat, such as chemical processing, marine environments, and high-temperature industrial equipment. The standard ensures uniform quality, consistent mechanical properties, and proper classification of nickel-based alloys intended for critical engineering use. ISO 4952 – Overview ISO 4952:2020 applies to hot-rolled flat products made from corrosion-resistant nickel-chromium-based alloys, offering guidance on chemical composition, mechanical characteristics, surface condition, and testing methods. The standard helps manufacturers and users of alloy materials meet performance demands in harsh environments. It supports product reliability by setting clear specifications for strength, ductility, resistance to oxidation, and dimensional tolerances. ISO 4952 also helps prevent failures due to improper material selection or insufficient resistance to aggressive operating conditions. ISO 4952:2020 Key Requirements Define mechanical properties such as tensile strength, yield strength, and elongation. Ensure proper chemical composition including nickel, chromium, iron, molybdenum, and other alloying elements. Maintain tight control on dimensional tolerances, thickness, and flatness. Ensure appropriate surface finish and absence of surface defects like cracks, pits, or scale. Follow specified heat treatment conditions to achieve required microstructure and mechanical properties. Conduct standardized testing such as tensile tests and hardness tests. Apply proper identification and marking for traceability of alloy grade and batch. Maintain documentation including material certificates and inspection reports. ISO 4952 Certification with Quality Asia Certification Quality Asia Certification provides ISO 4952:2020 certification to manufacturers of hot-rolled corrosion-resistant nickel-chromium alloy products. Certification validates that the alloy sheets, plates, and strips conform to international quality and safety standards. It assures customers and stakeholders of the material’s reliability and performance under demanding conditions, supporting its use in critical industries such as aerospace, power generation, and chemical processing. Certification Process for ISO 4952 Application Review – Analysis of product type, grade, and production capabilities. Stage 1 Audit – Evaluation of alloy specifications, quality documents, and test results. Stage 2 Audit – On-site assessment of manufacturing controls, testing labs, and product conformity. Certification Decision – Granting of ISO 4952 certificate after successful audit completion. Surveillance Audits – Annual assessments to ensure continual compliance and performance monitoring. Recertification – Full review every three years to maintain certification validity. Benefits of ISO 4952 Certification Assures product quality in corrosive and high-temperature environments. Strengthens trust among buyers, project engineers, and industry regulators. Supports access to global markets through standardized product specifications. Minimizes the risk of product failure in critical applications. Enhances manufacturing efficiency and product traceability. Demonstrates commitment to delivering high-performance alloy materials. Get ISO 4952 Certified with Us If your organization manufactures hot-rolled corrosion-resistant alloy products, ISO 4952:2020 certification helps ensure global recognition and reliable product performance. Quality Asia Certification offers globally accepted certification services to support your compliance with ISO 4952 standards. Contact us today to begin your ISO 4952 certification journey.
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  • ISO 4952 Certification Service

    ISO 4952 Certification Service

    25,000 / Set

    What is ISO 4952:2020? ISO 4952:2020 is an international standard that specifies the requirements for hot-rolled nickel-chromium-based corrosion-resistant alloy plate, sheet, and strip. These materials are commonly used in applications requiring high resistance to corrosion, oxidation, and heat, such as chemical processing, marine environments, and high-temperature industrial equipment. The standard ensures uniform quality, consistent mechanical properties, and proper classification of nickel-based alloys intended for critical engineering use. ISO 4952 – Overview ISO 4952:2020 applies to hot-rolled flat products made from corrosion-resistant nickel-chromium-based alloys, offering guidance on chemical composition, mechanical characteristics, surface condition, and testing methods. The standard helps manufacturers and users of alloy materials meet performance demands in harsh environments. It supports product reliability by setting clear specifications for strength, ductility, resistance to oxidation, and dimensional tolerances. ISO 4952 also helps prevent failures due to improper material selection or insufficient resistance to aggressive operating conditions. ISO 4952:2020 Key Requirements Define mechanical properties such as tensile strength, yield strength, and elongation. Ensure proper chemical composition including nickel, chromium, iron, molybdenum, and other alloying elements. Maintain tight control on dimensional tolerances, thickness, and flatness. Ensure appropriate surface finish and absence of surface defects like cracks, pits, or scale. Follow specified heat treatment conditions to achieve required microstructure and mechanical properties. Conduct standardized testing such as tensile tests and hardness tests. Apply proper identification and marking for traceability of alloy grade and batch. Maintain documentation including material certificates and inspection reports. ISO 4952 Certification with Quality Asia Certification Quality Asia Certification provides ISO 4952:2020 certification to manufacturers of hot-rolled corrosion-resistant nickel-chromium alloy products. Certification validates that the alloy sheets, plates, and strips conform to international quality and safety standards. It assures customers and stakeholders of the material’s reliability and performance under demanding conditions, supporting its use in critical industries such as aerospace, power generation, and chemical processing. Certification Process for ISO 4952 Application Review – Analysis of product type, grade, and production capabilities. Stage 1 Audit – Evaluation of alloy specifications, quality documents, and test results. Stage 2 Audit – On-site assessment of manufacturing controls, testing labs, and product conformity. Certification Decision – Granting of ISO 4952 certificate after successful audit completion. Surveillance Audits – Annual assessments to ensure continual compliance and performance monitoring. Recertification – Full review every three years to maintain certification validity. Benefits of ISO 4952 Certification Assures product quality in corrosive and high-temperature environments. Strengthens trust among buyers, project engineers, and industry regulators. Supports access to global markets through standardized product specifications. Minimizes the risk of product failure in critical applications. Enhances manufacturing efficiency and product traceability. Demonstrates commitment to delivering high-performance alloy materials. Get ISO 4952 Certified with Us If your organization manufactures hot-rolled corrosion-resistant alloy products, ISO 4952:2020 certification helps ensure global recognition and reliable product performance. Quality Asia Certification offers globally accepted certification services to support your compliance with ISO 4952 standards. Contact us today to begin your ISO 4952 certification journey.

    Type of Certification : ISO 4952

    Industry Focus : Diverse

    Certification Body Accreditation : NABCB

    Implementation Timeline : 20 days

    Cost : Based On Company Size & Complexity

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  • ISO 4951 Certification Service

    ISO 4951 Certification Service

    25,000 / Set

    • Type of CertificationISO 4951
    • Industry FocusDiverse
    • Certification Body AccreditationNABCB
    • Implementation Timeline20 days
    • CostBased On Company Size & Complexity
    • What is ISO 4951:2001? ISO 4951:2001 is an international standard that specifies the requirements for hot-rolled steel bars used in the production of mechanical springs. These steels are typically non-alloy or alloy steels with defined mechanical properties suitable for applications that require high fatigue strength, resilience, and dimensional accuracy. The standard ensures consistency in material quality for components like suspension springs, valve springs, and various industrial spring systems. ISO 4951 – Overview ISO 4951:2001 covers round, hot-rolled steel bars used for manufacturing springs subjected to dynamic loading and cyclic stress. The standard outlines classifications based on steel grades, heat treatment conditions, surface quality, and dimensional tolerances. It provides manufacturers and end-users with reliable guidelines to assess material performance before it is formed into finished spring products. ISO 4951 is widely used in the automotive, railway, aerospace, and machinery industries, where spring components must meet strict mechanical and safety requirements. ISO 4951:2001 Key Requirements Specify steel grades suitable for spring manufacturing based on chemical and mechanical properties. Control elements like carbon, manganese, silicon, chromium, and vanadium in defined limits. Ensure mechanical characteristics including tensile strength, yield strength, and elongation. Maintain precise dimensional tolerances and roundness for bar products. Check surface condition for defects such as seams, cracks, or scale that can impact fatigue life. Conduct hardness and microstructural testing to verify heat treatment effectiveness. Apply product identification with batch number, steel grade, and manufacturer details. Maintain traceability and records of test reports and material certifications. ISO 4951 Certification with Quality Asia Certification Quality Asia Certification offers ISO 4951:2001 certification services to steel manufacturers supplying hot-rolled bars for spring applications. Certification validates that your products meet the required international standards for metallurgical quality and mechanical performance. It ensures your spring steels are fit for high-load, high-performance applications, and comply with customer and industry requirements. Certification Process for ISO 4951 Application Review – Evaluation of product range, steel grades, and intended applications. Stage 1 Audit – Review of technical specifications, chemical and mechanical test reports, and quality documentation. Stage 2 Audit – On-site verification of production processes, inspection methods, and conformance to ISO 4951 requirements. Certification Decision – Granting of ISO 4951 certificate following successful audit closure. Surveillance Audits – Annual assessments to ensure consistent material quality and compliance. Recertification – Complete review every three years to maintain certification status. Benefits of ISO 4951 Certification Confirms compliance with global standards for spring steel quality. Supports acceptance by OEMs and global engineering firms. Reduces product failures by ensuring consistent mechanical performance. Enhances traceability and accountability in steel manufacturing. Promotes product reliability in fatigue-sensitive spring applications. Demonstrates commitment to quality in critical material supply. Get ISO 4951 Certified with Us If your organization manufactures hot-rolled steel bars for spring applications, ISO 4951:2001 certification helps assure clients of your material quality and process control. Quality Asia Certification provides trusted ISO certification services aligned with industry and regulatory standards. Contact us today to begin your ISO 4951 certification process.
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  • ISO 4951 Certification Service

    ISO 4951 Certification Service

    25,000 / Set

    What is ISO 4951:2001? ISO 4951:2001 is an international standard that specifies the requirements for hot-rolled steel bars used in the production of mechanical springs. These steels are typically non-alloy or alloy steels with defined mechanical properties suitable for applications that require high fatigue strength, resilience, and dimensional accuracy. The standard ensures consistency in material quality for components like suspension springs, valve springs, and various industrial spring systems. ISO 4951 – Overview ISO 4951:2001 covers round, hot-rolled steel bars used for manufacturing springs subjected to dynamic loading and cyclic stress. The standard outlines classifications based on steel grades, heat treatment conditions, surface quality, and dimensional tolerances. It provides manufacturers and end-users with reliable guidelines to assess material performance before it is formed into finished spring products. ISO 4951 is widely used in the automotive, railway, aerospace, and machinery industries, where spring components must meet strict mechanical and safety requirements. ISO 4951:2001 Key Requirements Specify steel grades suitable for spring manufacturing based on chemical and mechanical properties. Control elements like carbon, manganese, silicon, chromium, and vanadium in defined limits. Ensure mechanical characteristics including tensile strength, yield strength, and elongation. Maintain precise dimensional tolerances and roundness for bar products. Check surface condition for defects such as seams, cracks, or scale that can impact fatigue life. Conduct hardness and microstructural testing to verify heat treatment effectiveness. Apply product identification with batch number, steel grade, and manufacturer details. Maintain traceability and records of test reports and material certifications. ISO 4951 Certification with Quality Asia Certification Quality Asia Certification offers ISO 4951:2001 certification services to steel manufacturers supplying hot-rolled bars for spring applications. Certification validates that your products meet the required international standards for metallurgical quality and mechanical performance. It ensures your spring steels are fit for high-load, high-performance applications, and comply with customer and industry requirements. Certification Process for ISO 4951 Application Review – Evaluation of product range, steel grades, and intended applications. Stage 1 Audit – Review of technical specifications, chemical and mechanical test reports, and quality documentation. Stage 2 Audit – On-site verification of production processes, inspection methods, and conformance to ISO 4951 requirements. Certification Decision – Granting of ISO 4951 certificate following successful audit closure. Surveillance Audits – Annual assessments to ensure consistent material quality and compliance. Recertification – Complete review every three years to maintain certification status. Benefits of ISO 4951 Certification Confirms compliance with global standards for spring steel quality. Supports acceptance by OEMs and global engineering firms. Reduces product failures by ensuring consistent mechanical performance. Enhances traceability and accountability in steel manufacturing. Promotes product reliability in fatigue-sensitive spring applications. Demonstrates commitment to quality in critical material supply. Get ISO 4951 Certified with Us If your organization manufactures hot-rolled steel bars for spring applications, ISO 4951:2001 certification helps assure clients of your material quality and process control. Quality Asia Certification provides trusted ISO certification services aligned with industry and regulatory standards. Contact us today to begin your ISO 4951 certification process.

    Type of Certification : ISO 4951

    Industry Focus : Diverse

    Certification Body Accreditation : NABCB

    Implementation Timeline : 20 days

    Cost : Based On Company Size & Complexity

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  • ISO 4950 Certification Service

    ISO 4950 Certification Service

    25,000 / Set

    • Type of CertificationISO 4950
    • Industry FocusDiverse
    • Certification Body AccreditationNABCB
    • Implementation Timeline20 days
    • CostBased On Company Size & Complexity
    • What is ISO 4950:2014? ISO 4950:2014 is an international standard that specifies the technical delivery conditions for hot-rolled steel plates, wide flats, and sections intended for structural use in general engineering and construction. It includes requirements for weldable fine-grain structural steels with specified minimum yield strengths. The standard ensures the consistent mechanical and chemical properties of structural steel products used in critical applications, helping industries maintain quality, safety, and performance standards in structural fabrication. ISO 4950 – Overview ISO 4950:2014 classifies structural steels based on mechanical properties such as yield strength, tensile strength, and impact resistance. It covers steel grades used in bridges, buildings, industrial frameworks, shipbuilding, and other load-bearing applications. The standard includes requirements for heat treatment conditions, product form, and test methods to verify compliance. By adhering to ISO 4950, manufacturers and end-users ensure the steel components meet stringent international specifications, offering high structural integrity and safety assurance in construction projects. ISO 4950:2014 Key Requirements Specify yield strength and tensile strength based on steel grade and thickness. Meet defined values for elongation and Charpy V-notch impact energy. Control chemical composition including elements like carbon, manganese, phosphorus, and sulfur. Ensure flatness, surface condition, and dimensional tolerances of steel plates and sections. Perform non-destructive testing and visual inspections for surface defects. Apply appropriate heat treatment such as normalizing or thermomechanical rolling. Document material test reports, product certificates, and marking requirements. Comply with traceability and identification of steel products throughout production. ISO 4950 Certification with Quality Asia Certification Quality Asia Certification offers ISO 4950:2014 certification services to manufacturers and suppliers of hot-rolled structural steel products. Certification confirms that your products meet the specified mechanical and chemical properties required under international norms. It assures customers, regulators, and stakeholders that your structural steel materials are safe, compliant, and suitable for demanding construction and engineering projects. Certification Process for ISO 4950 Application Review – Initial assessment of product scope and steel grade categories. Stage 1 Audit – Verification of manufacturing controls, test records, and quality documentation. Stage 2 Audit – On-site inspection of production processes, testing methods, and product conformity. Certification Decision – Granting of ISO 4950 certificate upon successful audit completion. Surveillance Audits – Annual assessments to maintain ongoing compliance and quality standards. Recertification – Full system and product review every three years to renew certification. Benefits of ISO 4950 Certification Ensures product reliability and safety in structural applications. Strengthens market acceptance in construction and heavy engineering industries. Confirms compliance with international steel quality standards. Supports better material traceability and production control. Reduces project risks through consistent steel performance. Enhances brand credibility in domestic and export markets.   Get ISO 4950 Certified with Us If your organization produces or supplies hot-rolled structural steel, ISO 4950:2014 certification enhances your product value and global trust. Quality Asia Certification offers internationally recognized certification services to validate your steel products against stringent structural performance criteria. Contact us today to begin your ISO 4950 certification process
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  • ISO 4950 Certification Service

    ISO 4950 Certification Service

    25,000 / Set

    What is ISO 4950:2014? ISO 4950:2014 is an international standard that specifies the technical delivery conditions for hot-rolled steel plates, wide flats, and sections intended for structural use in general engineering and construction. It includes requirements for weldable fine-grain structural steels with specified minimum yield strengths. The standard ensures the consistent mechanical and chemical properties of structural steel products used in critical applications, helping industries maintain quality, safety, and performance standards in structural fabrication. ISO 4950 – Overview ISO 4950:2014 classifies structural steels based on mechanical properties such as yield strength, tensile strength, and impact resistance. It covers steel grades used in bridges, buildings, industrial frameworks, shipbuilding, and other load-bearing applications. The standard includes requirements for heat treatment conditions, product form, and test methods to verify compliance. By adhering to ISO 4950, manufacturers and end-users ensure the steel components meet stringent international specifications, offering high structural integrity and safety assurance in construction projects. ISO 4950:2014 Key Requirements Specify yield strength and tensile strength based on steel grade and thickness. Meet defined values for elongation and Charpy V-notch impact energy. Control chemical composition including elements like carbon, manganese, phosphorus, and sulfur. Ensure flatness, surface condition, and dimensional tolerances of steel plates and sections. Perform non-destructive testing and visual inspections for surface defects. Apply appropriate heat treatment such as normalizing or thermomechanical rolling. Document material test reports, product certificates, and marking requirements. Comply with traceability and identification of steel products throughout production. ISO 4950 Certification with Quality Asia Certification Quality Asia Certification offers ISO 4950:2014 certification services to manufacturers and suppliers of hot-rolled structural steel products. Certification confirms that your products meet the specified mechanical and chemical properties required under international norms. It assures customers, regulators, and stakeholders that your structural steel materials are safe, compliant, and suitable for demanding construction and engineering projects. Certification Process for ISO 4950 Application Review – Initial assessment of product scope and steel grade categories. Stage 1 Audit – Verification of manufacturing controls, test records, and quality documentation. Stage 2 Audit – On-site inspection of production processes, testing methods, and product conformity. Certification Decision – Granting of ISO 4950 certificate upon successful audit completion. Surveillance Audits – Annual assessments to maintain ongoing compliance and quality standards. Recertification – Full system and product review every three years to renew certification. Benefits of ISO 4950 Certification Ensures product reliability and safety in structural applications. Strengthens market acceptance in construction and heavy engineering industries. Confirms compliance with international steel quality standards. Supports better material traceability and production control. Reduces project risks through consistent steel performance. Enhances brand credibility in domestic and export markets.   Get ISO 4950 Certified with Us If your organization produces or supplies hot-rolled structural steel, ISO 4950:2014 certification enhances your product value and global trust. Quality Asia Certification offers internationally recognized certification services to validate your steel products against stringent structural performance criteria. Contact us today to begin your ISO 4950 certification process

    Type of Certification : ISO 4950

    Industry Focus : Diverse

    Certification Body Accreditation : NABCB

    Implementation Timeline : 20 days

    Cost : Based On Company Size & Complexity

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  • ISO 4920 Certification Service

    ISO 4920 Certification Service

    25,000 / Set

    • Type of CertificationISO 4920
    • Industry FocusDiverse
    • Certification Body AccreditationNABCB
    • Implementation Timeline20 days
    • CostBased On Company Size & Complexity
    • ISO 4920:2012 Certification – Spray Rating Test for Fabrics Overview ISO 4920:2012 is an international standard that specifies a test method to assess the water repellency of textile fabrics using the spray rating method. This standard helps evaluate the resistance of fabric surfaces to wetting by water, which is critical in applications where protection from water penetration is essential, such as in rainwear, outdoor apparel, and performance textiles. What is ISO 4920:2012? ISO 4920:2012, titled "Textiles — Determination of resistance to surface wetting (spray test) ", outlines a procedure to determine how well a fabric can resist water penetration under specific conditions. The test involves spraying water on the surface of the fabric and comparing the wetting pattern to a standardized rating scale. This non-absorption test is suitable for various types of fabrics treated with water-repellent finishes or those designed for outdoor use. Why ISO 4920:2012 Certification? Obtaining ISO 4920:2012 certification signifies that a textile product has been tested for its ability to repel water on the surface. This certification is important for manufacturers and suppliers who aim to meet international quality standards in the textile industry. It enhances product reliability, improves buyer confidence, and meets the functional requirements for garments and textiles exposed to moisture or wet conditions. Requirements for ISO 4920:2012 Certification To undergo ISO 4920:2012 certification, organizations must: Ensure fabric samples are prepared and finished as per the intended end-use. Maintain proper conditioning of the sample in a standardized environment. Follow the testing procedure using a standard spray tester and rating chart. Maintain proper documentation of test results and conformity reports. Demonstrate consistency in water-repellent performance across production batches. Certification Process Application Submission – Client submits the request for ISO 4920:2012 certification along with product details. Document Review – Evaluation of sample preparation, treatment methods, and testing environment compliance. Sample Testing – Fabric samples are tested as per ISO 4920:2012 methodology under controlled laboratory conditions. Technical Evaluation – Analysis of the test results and comparison with standard spray rating scale. Certificate Issuance – Upon satisfactory results, the ISO 4920:2012 certificate is issued with defined validity. Surveillance (if applicable) – Periodic checks to ensure product consistency, as agreed in certification terms. Benefits of ISO 4920:2012 Certification   Enhanced Product Quality – Validates fabric resistance to water wetting, proving suitability for outdoor and protective use. Improved Customer Trust – Certification serves as proof of performance and quality assurance for buyers. Market Competitiveness – Facilitates entry into international markets where water-repellent standards are mandatory. Regulatory Compliance – Meets requirements set by industries using technical textiles and performance apparel. Reduced Product Returns – Minimizes complaints and returns due to ineffective water resistance in fabric.
    ...more
  • ISO 4920 Certification Service

    ISO 4920 Certification Service

    25,000 / Set

    ISO 4920:2012 Certification – Spray Rating Test for Fabrics Overview ISO 4920:2012 is an international standard that specifies a test method to assess the water repellency of textile fabrics using the spray rating method. This standard helps evaluate the resistance of fabric surfaces to wetting by water, which is critical in applications where protection from water penetration is essential, such as in rainwear, outdoor apparel, and performance textiles. What is ISO 4920:2012? ISO 4920:2012, titled "Textiles — Determination of resistance to surface wetting (spray test) ", outlines a procedure to determine how well a fabric can resist water penetration under specific conditions. The test involves spraying water on the surface of the fabric and comparing the wetting pattern to a standardized rating scale. This non-absorption test is suitable for various types of fabrics treated with water-repellent finishes or those designed for outdoor use. Why ISO 4920:2012 Certification? Obtaining ISO 4920:2012 certification signifies that a textile product has been tested for its ability to repel water on the surface. This certification is important for manufacturers and suppliers who aim to meet international quality standards in the textile industry. It enhances product reliability, improves buyer confidence, and meets the functional requirements for garments and textiles exposed to moisture or wet conditions. Requirements for ISO 4920:2012 Certification To undergo ISO 4920:2012 certification, organizations must: Ensure fabric samples are prepared and finished as per the intended end-use. Maintain proper conditioning of the sample in a standardized environment. Follow the testing procedure using a standard spray tester and rating chart. Maintain proper documentation of test results and conformity reports. Demonstrate consistency in water-repellent performance across production batches. Certification Process Application Submission – Client submits the request for ISO 4920:2012 certification along with product details. Document Review – Evaluation of sample preparation, treatment methods, and testing environment compliance. Sample Testing – Fabric samples are tested as per ISO 4920:2012 methodology under controlled laboratory conditions. Technical Evaluation – Analysis of the test results and comparison with standard spray rating scale. Certificate Issuance – Upon satisfactory results, the ISO 4920:2012 certificate is issued with defined validity. Surveillance (if applicable) – Periodic checks to ensure product consistency, as agreed in certification terms. Benefits of ISO 4920:2012 Certification   Enhanced Product Quality – Validates fabric resistance to water wetting, proving suitability for outdoor and protective use. Improved Customer Trust – Certification serves as proof of performance and quality assurance for buyers. Market Competitiveness – Facilitates entry into international markets where water-repellent standards are mandatory. Regulatory Compliance – Meets requirements set by industries using technical textiles and performance apparel. Reduced Product Returns – Minimizes complaints and returns due to ineffective water resistance in fabric.

    Type of Certification : ISO 4920

    Industry Focus : Diverse

    Certification Body Accreditation : NABCB

    Implementation Timeline : 20 days

    Cost : Based On Company Size & Complexity

    ...more
    Get Best Price
  • ISO 4892 Certification Service

    ISO 4892 Certification Service

    25,000 / Sets

    • Type of CertificationISO 4892
    • Industry FocusDiverse
    • Certification Body AccreditationNABCB
    • Implementation Timeline20 days
    • CostBased On Company Size & Complexity
    • What is ISO 4892-1:2016? ISO 4892-1:2016 is an international standard that outlines the general principles for the exposure of plastic materials to laboratory light sources. This standard serves as the foundational part of a multi-part series that specifies methods to simulate the effects of natural and artificial weathering on plastics. It plays a crucial role in determining a material’s resistance to degradation from light, heat, and moisture—factors that significantly impact the long-term durability and appearance of plastic products. ISO 4892 – Overview Part 1 of ISO 4892 establishes the basic requirements and testing framework used across the other parts in the series, including methods involving xenon-arc lamps, fluorescent UV lamps, and open-flame carbon-arc sources. It defines test conditions, sample preparation guidelines, performance evaluation techniques, and reference standards to ensure uniformity in test application. This standard is essential for manufacturers who need to evaluate the weatherability of plastic materials used in outdoor applications such as construction, automotive parts, signage, and consumer goods. ISO 4892:2016 Key Requirements Defines standardized laboratory procedures to simulate the aging effects of sunlight and moisture on plastics. Specifies general guidance for exposure apparatus, sample positioning, and operational conditions. Establishes procedures for evaluating property changes such as discoloration, cracking, embrittlement, or loss of strength. Outlines parameters for temperature, humidity, radiation intensity, and exposure cycles. Includes recommendations for pre-conditioning of test specimens. Provides criteria for reference materials and inter-laboratory consistency. Requires documentation of equipment calibration, test duration, and any deviations from the standard method. Ensures that results are comparable across different test methods specified in ISO 4892-2 to ISO 4892-4. ISO 4892 Certification with Quality Asia Certification Quality Asia Certification offers ISO 4892-1:2016 certification services to manufacturers and testing laboratories handling plastic products. Certification ensures that your materials are tested under controlled and internationally recognized conditions for UV resistance, aging, and weather durability. It verifies your compliance with product quality and performance expectations for markets where exposure to sunlight and environmental stress is a concern. Certification Process for ISO 4892 Application Review – Evaluation of product types, exposure requirements, and test method relevance. Stage 1 Audit – Review of testing procedures, calibration records, and environmental controls. Stage 2 Audit – On-site inspection of equipment setup, sample handling, and compliance with ISO 4892 guidelines. Certification Decision – Issuance of ISO 4892-1:2016 certificate upon successful audit verification. Surveillance Audits – Annual assessments to confirm consistent test quality and equipment maintenance. Recertification – Full review every three years to ensure ongoing compliance with ISO 4892 standards. Benefits of ISO 4892 Certification Demonstrates material performance under simulated real-world environmental conditions. Supports quality assurance in industries where UV resistance and durability are critical. Enhances customer trust by validating weatherability claims with standardized methods. Reduces risk of product failure due to exposure-related degradation. Improves product design and development with reliable test data. Facilitates international market acceptance through recognized certification.   Get ISO 4892 Certified with Us If your organization produces or tests plastic materials for outdoor or UV-exposed applications, ISO 4892-1:2016 certification confirms adherence to globally accepted testing practices. Quality Asia Certification provides ISO certification services to help your materials meet durability and weatherability expectations. Contact us to
    ...more
  • ISO 4892 Certification Service

    ISO 4892 Certification Service

    25,000 / Sets

    What is ISO 4892-1:2016? ISO 4892-1:2016 is an international standard that outlines the general principles for the exposure of plastic materials to laboratory light sources. This standard serves as the foundational part of a multi-part series that specifies methods to simulate the effects of natural and artificial weathering on plastics. It plays a crucial role in determining a material’s resistance to degradation from light, heat, and moisture—factors that significantly impact the long-term durability and appearance of plastic products. ISO 4892 – Overview Part 1 of ISO 4892 establishes the basic requirements and testing framework used across the other parts in the series, including methods involving xenon-arc lamps, fluorescent UV lamps, and open-flame carbon-arc sources. It defines test conditions, sample preparation guidelines, performance evaluation techniques, and reference standards to ensure uniformity in test application. This standard is essential for manufacturers who need to evaluate the weatherability of plastic materials used in outdoor applications such as construction, automotive parts, signage, and consumer goods. ISO 4892:2016 Key Requirements Defines standardized laboratory procedures to simulate the aging effects of sunlight and moisture on plastics. Specifies general guidance for exposure apparatus, sample positioning, and operational conditions. Establishes procedures for evaluating property changes such as discoloration, cracking, embrittlement, or loss of strength. Outlines parameters for temperature, humidity, radiation intensity, and exposure cycles. Includes recommendations for pre-conditioning of test specimens. Provides criteria for reference materials and inter-laboratory consistency. Requires documentation of equipment calibration, test duration, and any deviations from the standard method. Ensures that results are comparable across different test methods specified in ISO 4892-2 to ISO 4892-4. ISO 4892 Certification with Quality Asia Certification Quality Asia Certification offers ISO 4892-1:2016 certification services to manufacturers and testing laboratories handling plastic products. Certification ensures that your materials are tested under controlled and internationally recognized conditions for UV resistance, aging, and weather durability. It verifies your compliance with product quality and performance expectations for markets where exposure to sunlight and environmental stress is a concern. Certification Process for ISO 4892 Application Review – Evaluation of product types, exposure requirements, and test method relevance. Stage 1 Audit – Review of testing procedures, calibration records, and environmental controls. Stage 2 Audit – On-site inspection of equipment setup, sample handling, and compliance with ISO 4892 guidelines. Certification Decision – Issuance of ISO 4892-1:2016 certificate upon successful audit verification. Surveillance Audits – Annual assessments to confirm consistent test quality and equipment maintenance. Recertification – Full review every three years to ensure ongoing compliance with ISO 4892 standards. Benefits of ISO 4892 Certification Demonstrates material performance under simulated real-world environmental conditions. Supports quality assurance in industries where UV resistance and durability are critical. Enhances customer trust by validating weatherability claims with standardized methods. Reduces risk of product failure due to exposure-related degradation. Improves product design and development with reliable test data. Facilitates international market acceptance through recognized certification.   Get ISO 4892 Certified with Us If your organization produces or tests plastic materials for outdoor or UV-exposed applications, ISO 4892-1:2016 certification confirms adherence to globally accepted testing practices. Quality Asia Certification provides ISO certification services to help your materials meet durability and weatherability expectations. Contact us to

    Type of Certification : ISO 4892

    Industry Focus : Diverse

    Certification Body Accreditation : NABCB

    Implementation Timeline : 20 days

    Cost : Based On Company Size & Complexity

    ...more
    Get Best Price

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About the Company

  • Primary Business Service Provider
  • Secondary Business Type Manufacturer
  • Year of Establishment 2021
  • No. of Employees 21 - 50
  • Annual Turnover Rs. 0.5 to 2.5 Crore Approx.
  • Ownership Type LLC (Ltd Liability Corp)

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Quality Asia, headquartered in India, is a global leader in auditing, inspection, and certification services. We offer 24/7 state-of-the-art audits using industry-leading methods and a customer-first approach. Our global accreditations and alliances make us the preferred partner for regulatory, market, and supply chain compliance.
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Quality Asia

  • Mr Parveen Singh Negi
  • 212 Bhera Enclave, Paschim Vihar, Delhi - 110087, Peeragarhi
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