ISO Certification Services

An ISO registration is an essential certification which enhances the reputation of the service and the products that your organisation supplies to your clients. There are different types of ISO certification that you can apply to your business. So if you want ISO 9001 2015 Certification Services for your organization or business, contact us at Mark Certification Services. If you are thinking about why us? Here are some reasons for it. Our experts will help you get the right information about ISO. You will get assistance while you fill-up the application and we will help you entire the process of application. We will help you search comprehensive and quality policy standards so that you don’t have any issue.

• ISO 17020 Accredited Inspection Agency: ISO 17025 Accredited Testing Laboratory

ISO 13485:2016 specifies requirements for a quality management system where an organization needs to demonstrate its ability to provide medical devices and related services that consistently meet customer and applicable regulatory requirements. Such organizations can be involved in one or more stages of the life-cycle, including design and development, production, storage and distribution, installation, or servicing of a medical device and design and development or provision of associated activities (e.g. technical support). ISO 13485:2016 can also be used by suppliers or external parties that provide product, including quality management system-related services to such organizations. ISO 13485 is a quality management standard for the manufacturers of medical devices. Obviously, medical device producers must be able to provide evidence that their devices consistently meet safety and quality standards as well as perform as intended for patients or consumers. ISO 13485 provides an international approach to meeting the wide-ranging requirements of medical device production and related services for the world market. If applicable regulatory requirements permit exclusions of design and development controls, this can be used as a justification for their exclusion from the quality management system. These regulatory requirements can provide alternative approaches that are to be addressed in the quality management system. It is the responsibility of the organization to ensure that claims of conformity to ISO 13485:2016 reflect any exclusion of design and development controls.  If any requirement in Clauses 6, 7 or 8 of ISO 13485:2016 is not applicable due to the activities undertaken by the organization or the nature of the medical device for which the quality management system is applied, the organization does not need to include such a requirement in its quality management system.  COMPLIANCE & CERTIFICATION STEPS  Preliminary Audit (Optional): During preliminary assessment, CDG reviews\ inspects your site to check documentation & implementation of quality management system for your organization, based on ICMED and ISO 13485 requirements.  Phase 1 - Initial Certification Audit (Mandatory): CDG audits your site to determine that your organization is in compliance with the standard and ready for certification audits based on ISO 13485 and additional requirements of ICMED 13485.  Phase 2 - Initial Certification Audit (Mandatory): Based on phase 1 outcomes, CDG does on-site certification audit to evaluate implementation and compliance of standard effectively and in a continuous manner.  ICMED & ISO 13485 Certificate: Based on satisfactory phase 2 audit outcomes, CDG will issue a certificate confirming compliance with standards.  BENEFITS  ICMED 13485 and ICMED 9000 certification from CDG allows you to:  Communicate high standards of your product quality in the medical device industry  Gain a competitive edge with independent certification scheme  Build a qualified team of local auditors & reviewers with global auditing experience, based on ISO 13485 standard 

• Country of Origin: India
• Certification: ISO 17712
• ISO 17020 Accredited Inspection Body: ISO 17025 Accredited Testing Laboratory

CDG is an ISO 17021 accredited inspection body & ISO 17025 accredited testing laboratory for ISO 17712 standards. We provide accredited ISO 17712 certification services in Kolkata.The ISO 17712 establishes “uniform procedures for the classification, acceptance, and withdrawal of mechanical freight container seals. It provides a single source of information on mechanical seals which are acceptable for securing freight containers in international commerce.” The current ISO 17712 standard requires independent confirmation in three areas: 1. Testing to determine a seal’s physical strength (as barriers to entry). ISO 17712 defines three types of classes of seal strength or barrier capacity: “I” for Indicative; “S” for Security; and “H” for High Security. C-TPAT requires the use of “H” class seals. Suppliers must use independent third party test laboratories to validate a seal's classification. Labs must be accredited according to ISO/IEC 17025 (General requirements for the competence of testing and calibration laboratories) to perform testing specific to ISO 17712. 2. Auditing of manufacturer’s security-related business processes. Poor security-related practices can undercut the effectiveness of a high-quality security seal. ISO 17712's Annex A defines over two dozen required practices, such as facility risk assessments and access controls to production and storage areas. Suppliers’ conformance with Annex A should also be demonstrated through an independent certification provider that is accredited to audit compliance with the ISO standards. 3. Seals be designed and constructed with tamper indicative features that generate tell-tale evidence of tampering. Seal manufacturers must be able to demonstrate to, and obtain certification from, an accredited auditor from an independent third-party organization that their high security seals have built-in tamper evidence features. If an independent third-party organization accredited to ISO 17020 verifies conformity, it will provide the manufacturer with a certificate of compliance that documents that the seals submitted for review do reflect tell-tale evidence of tampering generated by attempts to defeat a correctly closed and affixed seal. Considering that most seals are tampered with in order to introduce illegal contraband or to pilferage a container, this is a welcomed improvement for high security seals –particularly those that are U.S. bound and those affixed to C-TPAT containers and trailers. C-TPAT’s security criteria states that a high security seal must be affixed to all loaded containers bound for the U.S. All seals must meet or exceed the current ISO 17712 standards for high security seals.” C-TPAT Partners, however, may continue to use the remaining ISO 17712:2010 high security seals they have in stock and then look to purchase ISO 17712:2013 high security seals in the future. ISO 17712 is the standardised document that establishes “uniform procedures for the classification, acceptance, and withdrawal of mechanical freight container seals. It provides a single source of information on mechanical seals which are acceptable for securing freight containers in international commerce.” ISO 17712 defines three types of classes of security seal strength, or barrier capacity: “I” for Indicative; “S” for Security; and “H” for High Security. C-TPAT requires the use of “H” class seals. Suppliers must use independent third party test laboratories to validate a security seal’s classification. The test laboratory must also be accredited according to ISO/IEC 17025 (General requirements for the competence of testing and calibration laboratories) to perform testing specific to ISO 17712.

Location/City Pan India Type of Certification Renewal Type Of Industry Manufacturing Type Of Service Provider Consulting Firm Established in the year 2000, at Mumbai, Maharashtra, India, we “Deming Certification Services Pvt. Ltd.,” offer clients total certifications solutions that helps in enhancing systems and processes at their end. Further, the expertise of certifications personnel also assist us in changing the working pattern of several organizations by bringing positive change in their work culture as well as inculcating quality in every sphere of involved operations.   The solutions offered by us cover areas like ISO 9001 Certification, ISO 27001 Certification, ISO 14001 Certification, SQC/SPC  Certification, ISO 17025  Certificationand ISO 22000 Certification. Apart from this, we also offer solutions for HACCPCertification, ISO/TS 16949 Certification, OHSAS 18001, Social Accountability Certification, Risk Assessment Services, ISO 20000 Certification, Project Management Certification, SA 8001 Certificationand Third Party Inspection and Verification Services.   Our business operations are led by Mr. Mukesh Singh, who has with him rich experience in our industry sector. His visionary approach has also assisted us in emerging amongst fastest growing business management certification companies in our industry sector. Further, the service support provided by experienced industry professionals also allow us to offer clients a wide range of business certifications services for availing different certifications.   Today, our team of experts work in close coordination with clients and help them to access their specific requirements as well as add value to their systems. This is achieved through designing formats as well as assisting in implementation by continuous training, review of quality manual as well as undertaking other allied procedures. Other than this, the competitive prices of our services also makes them one of the most demanded in the market.

ISO 31000 provides principles and generic guidelines to assist organizations in establishing, implementing, operating, maintaining and continually improving their risk management framework. It is not specific to any industry or sector, so it can be used by any public, private or community enterprise, association, group or individual. This standard can be applied throughout the life of an organization, and to a wide range of activities, including strategies and decisions, operations, processes, functions, projects, products, services and assets. This standard is not intended to promote uniformity of risk management across organizations. The design and implementation of risk management plans and frameworks will need to take into account the varying needs of a specific organization, its particular objectives, context, structure, operations, processes, functions, projects, products, services, or assets and specific practices employed. ISO 31000 is organized into the following main clauses: Clause 3: Principles Clause 4: Framework Clause 5: Process   Each of these key activities is listed below. Clause 3: Principles of risk management  In order to have an effective risk management, an organization has to comply with these 11 principles.   Risk management creates and protects value; Risk management is an integral part of all organizational processes; Risk management is part of decision making; Risk management explicitly addresses uncertainty; Risk management is systematic, structured and timely; Risk management is based on the best available information; Risk management is tailored; Risk management takes human and cultural factors into account; Risk management is transparent and inclusive; Risk management is dynamic, iterative and responsive to change; Risk management facilitates continual improvement of the organization. Clause 4: Framework  ISO 31000 states that the success of risk management will depend on the effectiveness of the management framework providing the foundations and arrangements what will embed it throughout the organization at all levels. The framework: assists in managing risks effectively through the application of the risk management process; ensures that information about risk derived from the risk management process is adequately reported; and ensures that these information is used as a basis for decision making and accountability at all relevant organizational levels. This clause describes the necessary components of the framework for managing risk and the way in which they interrelate in an iterative manner. Design of framework for managing risk: Before the implementation, the organization must design a framework for managing risk. This includes:    Understanding of the organization and its context  Establishing risk management policy  Ensuring accountability, authority and appropriate competence for risk management  Integrating risk management into organizational processes  Allocating appropriate resources  Establishing internal and external communication and reporting mechanisms ISO 31000 states that the success of risk management will depend on the effectiveness of the management   The risk management process should be: An integral part of management; Embedded in the culture and practices; Tailored to the business processes of the organization.  Risk management process comprises the following activities:

Elevate your business standards with our ISO Certification service. We guide you through the certification process, ensuring compliance with international quality, safety, and efficiency standards. Our expert consultants provide comprehensive assistance, from documentation to implementation, ensuring a seamless ISO certification journey. Gain a competitive edge, enhance customer trust, and improve operational excellence with our tailored ISO solutions. We cater to various ISO standards, adapting our services to your industry-specific needs. Join the ranks of globally recognized, quality-focused businesses. Choose our ISO Certification service for a reliable, efficient, and strategic approach to demonstrating your commitment to excellence and continuous improvement.

Food safety is related to the presence of food-borne hazards in food at the point of consumption (intake by the consumer). As the introduction of food safety hazards can occur at any stage of the food chain, adequate control throughout the food chain is essential. Food safety is ensured through combined efforts of all parties participating in the food chain. ISO 22000 specifies requirements for a food safety management system that combines elements such as interactive communication, system management, prerequisite programmes and HACCP principles.   The process As an organisation, the steps involved for you are:   Applying for certification: Review and accept our customised Proposal, and you’re underway! Achieving certification: Firstly, a pre-certification audit or “test run” will be conducted either on-site (at your premises) or off-site (at our premises) or both, to see whether your management systems are suitable. Areas of concern will be reported. Once concerns have been actioned, an on-site certification audit will be conducted, where we will examine the extent to which you address the program criteria. Areas of concern will be reported. Once we are satisfied there are no outstanding issues that present an unacceptable risk to you, your employees, customers, regulators, Equal Assurance or others, we can proceed to issue a Certificate of Confidence. Well done! Maintaining certification: Depending on the level of risk, we will conduct a series of surveillance audits (and in some cases special and follow-up audits) and tri-ennial re-certification audits, to examine the extent to which you continue to address the program criteria. Areas of concern will be reported. So long as we continue to be satisfied there are no outstanding issues that present an unacceptable risk to you, your employees, customers, regulators, Equal Assurance or others, your certification remains valid.

• Country of Origin: India
• Payment Mode: Advance
• Type Of Ownership: proprietor
• Dose/Strength: 200 mg
• Usage/Application: Personal < Hospital < Clinical
• Packaging Size: 1x15

Brand name of this medicine is Pirfenex . Pirfenex  medicine contains generic Pirfenidone . Pirfenidone are available in form of Tablet. Each Coated Tablet contains 200Mg Pirfenidone. One Pack of Pirfenex 30 Tablets. Manufacturer & Marketed company name of Pirfenex  is Cipla Pharma Ltd, India.   USED - Pirfenex Tablet is used in the treatment of idiopathic pulmonary fibrosis.     Dosage- As directed by the physician.   Details- 1.         Brand name – Pirfenex 2.         Generic - Pirfenidone 3.         Strength – 200 Mg 4.         Dosage form – Tablets 5.         Used –  It is used in the treatment of idiopathic pulmonary fibrosis. 6.         Packaging – 30 Tablets 7.         Manufactured & Marketed By –  Cipla Pharma Ltd 8.         Delivery time – 4 to 7 days (worldwide) & 24 hours to 48 hours (India)   Delivery process - We can ship your medicine worldwide within 4-12 days through E.M.S. - Express mail service.   Warning: Pirfenex medicine  is a prescription drug and should be used under proper medical guidance and advice. Do not share the medicine with others, since they may be suffering from a problem that is not effectively treated by this drug.   • Keep all medicines out of the reach of children and away from pets, never share your medicines with others, and use this medication only for the indication prescribed.   • The information contained herein is not intended to cover all possible uses, directions, precautions, warnings, drug interactions, allergic reactions, or adverse effects. If you have questions about the drugs you are taking, check with your doctor, nurse or pharmacist.   Notice: The above information is an educational aid only. It is not intended as medical advice for individual conditions or treatments. Talk to your doctor, nurse or pharmacist before following any medical regimen to see if it is safe and effective for you.   Before eating/consuming any medicine kindly do consult with your doctor / Medical adviser / Nurse / Hospital /medicine Institution / Health advisor or pharmacist/ medicine healer.   Do not indulge in self medication using internet information.   Self medication can be dangerous.

What is ISO 22163:2017The International Organization for Standardization has published guidelines to bring a quality management approach to the rail sector.ISO/TS 22163, Railway applications – Quality management system – Business management system requirements for rail organizations: ISO 9001:2015 and particular requirements for application in the rail sector, aims to help system integrators and equipment manufacturers in the rail sector make quality improvements through common best practices.The technical specification is a sector-specific application of ISO 9001:2015 and was developed in collaboration with the Association of the European Rail Industry to build on its industry standard.ISO/TS 22163 defines quality management system requirements for the rail sector that can be applied throughout the supply chain—including design and development, manufacturing, and maintenance.In October 2016, the Association of the European Rail Industry, UNIFE, announced the decision of Technical Committee 269 of the International Organization for Standardization (ISO) to replace the global standard for quality management systems in the rail industry – IRIS Rev. 02 – by a new ISO/TS 22163 version. Consequently, organisations certified according to IRIS Rev. 02 will have to undergo transition audits to update their certificates to ISO/TS 22163. ISO/TS 22163 will be based on the structure and requirements of the ISO 9001:2015 standard, which it will adopt in full, but comprises additional requirements for the rail industry. Deadlines and schedule Publication of the ISO/TS 22163 and the associated certification rules is scheduled for May 2017. Following the publication of the new standard, organisations are required to implement the changes in their quality management system prior to a transition audit. Certification auditors seeking to carry out audits according to ISO/TS 22163 are required to attend, and successfully complete, training supervised by UNIFE. On this background, July/August 2017 is a realistic timeline for the first transition audits. As IRIS Rev.02 certificates will expire after 14 September 2018, and all non-conformities need to be closed for all audits before a new ISO/TS 22163 certificate can be issued, the last transition audits should be completed by July 2018. Regulation for the auditing of remote locations/ support functions and extended workbenches/ site extensions Since the quality management system of ISO/TS 22163 takes an integrated approach to the organisations and/ or the production site, the transition of the quality management system to ISO/TS 22163 at remote locations/support functions and extended workbenches/ site extensions must be completed before the transition audit takes place. As was the case for former regulations, remote locations/support functions must be audited prior to the associated production site(s). This principle continues to apply for the transition phase from IRIS Rev. 02 to ISO/TS 22163.The new ISO/TS 22163: 2017 standard:Is published in May 2017 and replaced the existing IRIS Rev.2.01, till September  2018, covers all requirements of ISO 9001:2015 and has been built according to the High Level Structure, supplemented by existing and new additional mandatory and optional requirements of the rail industry especially also new KPIs,continues to be supported by the "IRIS Audit Tool" that is based on the new IRIS Assessment Sheet, composed by around 870 mandatory requirements, which are grouped into about 300 questions, as well as new KO-requirements (plus additional optional requirements), Requires the appraisal of the customer focus performance level,Requires introduction of turtle diagrams and applies the methodology of Process Effectiveness Assessment Reviews (PEAR) for some mandatory processes, Utilizes a maturity model for business management systems concluding your companies BRONZE-SILVER-GOLD rating.Role of ConsultantAssisting to client from beginning till certification that includes documentation, training and internal auditing.

We are service providers of iso certification services. We offer wide range of consulting services for system & product certification like iso 9001, iso 27001,iso 20000, iso 14001, ohsas 18001, iso 22000, haccp, sqc, brc, fssc 22000, ts 16949, iso 13485, iso 50001,ce certification, sa 8000, sedex, bsci, social compliances etc. We provide iso certification consulting, training and implementation services in the all cities of india.our aim to assist various business entities to define, implements, and improve their structure based on iso standards.

This course is designed for persons in top management team of the organization. Certificate would be provided to persons stating participation in above course.Course content: All requirements of ISO 9001 under the leadership Clause. Also included is how the organization review the performance and monitor effectiveness of QMS implementation. management (Quality Management System). The same course can be repeated for Each one of the standards namely, 9001, 14001, 45001 & 50001.Next Step Register for the course by filling up following details. (as per attachment). Attend course and get certificate. Course Fee Per person₹1180 /US $ 15    

ISO certification helps to boost your business quality additionally the overall potency of thebusiness. ISO is an independent organization that gives standards in terms of quality, safety,and efficiency of products and services provided by businesses. With the increasingcompetition among the business, it’s top of the notch to deliver top quality of goods &amp;services so as to sustain within the market.  ISO 9001 CERTIFICATION - QUALITY MANAGEMENT SYSTEM  ISO 14001 CERTIFICATION – ENVIRONMENTAL MANAGEMENT SYSTEM (EMS)  ISO 27001 CERTIFICATION - INFORMATION SECURITY  ISO 45001:2018 CERTIFICATION – OH&amp;S CERTIFICATION (OCCUPATIONAL HEALTH AND SAFETY MANAGEMENT SYSTEM)  ISO 22000:2018 CERTIFICATION – FOOD SAFETY MANAGEMENT SYSTEM (FSMS)- FSSC22000 Certification  ISO 20000:2018 CERTIFICATION – IT SERVICE MANAGEMENT SYSTEM Other Certification  CE certification for Medical Devices and Machines  BIS registration for Electronic and Electrical Devices  HACCP: Food Safety Management -- Hazard Analysis and Critical Control Points (HACCP)  KOSHER (Just as the Food and Drug Administration inspects the US food supply to ensure that it is safe to eat and free from contamination according to US laws, Kosher certification agencies like EarthKosher inspect and certify food as well, in keeping with Jewish dietary laws.) SEDEX Certification -is a globally recognized accreditation that signifies a company’s commitment to ethical and responsible sourcing and manufacturing practices. It is a mark of trust that indicates a company’s dedication to social and environmental responsibility. SA8000-- The SA8000 Standard is an auditable certification standard thatencourages organizations to develop, maintain, and apply socially acceptable practices in the workplace. It was developed in 1989 by Social Accountability International, formerly the Council on Economic Priorities, by an advisory board consisting of trade unions, NGOs, civil society organizations and companies.The SA8000&#39;s criteria were developed from various industry and corporate codes to create a common standard for social welfare compliance. The current (2014) version of the standard is built on earlier 2001, 2004 and 2008 versions.

ISO 13485:2003 specifies requirements for a quality management system where an organization needs to demonstrate its ability to provide medical devices and related services that consistently meet customer requirements and regulatory requirements applicable to medical devices and related services.

Chirag Group Of Company is a Kolkata (West Bengal, India) based company, which is indulged in providing superior class ISO registration services to the clients. To get your company registered under ISO and getting the certification of genuine standardization and quality assurance of your products & services, you need to register under ISO. Our team members are experts in assisting various clients in completing all the major operations to register under ISO.

We offer iso certificate. This is now a iso 9001:2008 certified company.

• Type of Certification: New Certification
• Service Mode: Online
• Payment Mode: Online/Offline
• Type Of Ownership: Proprietorship
• Country of Origin: India
• Application: License

Elevate your business standards with our ISO Registration Service. Our expert team ensures efficient certification processes for ISO standards, enhancing your organization's credibility. We specialize in ISO 9001, 14001, and other quality management systems, offering meticulous documentation and compliance adherence. Trust us for a hassle-free registration experience, allowing you to focus on excellence in your operations. Partner with us to secure ISO Registration efficiently, signaling to clients and stakeholders your commitment to quality and continual improvement in business practices.  

Prioritize workplace safety and employee well-being with ISO 45001 Certification Services. Our expert guidance ensures a seamless certification process, emphasizing your commitment to occupational health and safety. Achieve ISO 45001 certification, a globally recognized standard, signaling excellence in managing occupational risks. Streamline safety processes, reduce workplace incidents, and foster a culture of well-being. Opt for ISO 45001 Certification Services to enhance your organizational resilience, comply with regulations, and demonstrate a proactive approach to employee safety. Choose a safer future for your workplace with our comprehensive certification support, reinforcing your commitment to a secure and healthy work environment.

E- Filling Infotech Private Limited is a known name, specialized in providing ISO certification services from Kolkata (West Bengal, India). With our services, we assist clients to prepare for the implementation of the ISO standards, filling & filing application, audits, and completing other related formalities in a careful manner. We majorly cater to ISO certifications requirements of clients across IT and Consulting, Manufacturing, Banking, and Finance sectors. To schedule an appointment with one of our consultants, ring us on the given numbers.

ISO certification services validate an organization's commitment to quality, efficiency, and customer satisfaction. Achieving ISO certification signifies adherence to international standards, enhancing credibility and market competitiveness. These certifications cover various aspects, such as quality management, environmental practices, and information security. Organizations undergo rigorous assessments to meet ISO requirements, ensuring robust systems and processes. ISO certification is a globally recognized hallmark, attracting customers and stakeholders, and demonstrating a dedication to excellence in products or services.

Listed amid the celebrated names in the industry, we are providing ISO certification consultancy services to the businesses in the city. Ours is a group of skilled professionals, who work together & with clients and provide solutions as per their needs. With this, we help them in completing the paperwork and other legal procedures. We are operating from Nanded (Maharashtra, India); clients can get in touch with anytime, through our website. Our service charges are also reasonable.

In agreement with the stellar reputation of ours, we offer our esteemed clients a varied range of services of ISO Certificate Registration Services. We are committed towards meeting our clients precise needs. Our service is far and wide availed for its consistency & affordability. Our accomplished staff provides consultation to the clients regarding the whole registration process. The service is provided as per the specifications given by clients. Other than that, our service is highly appreciated for timely execution among our clients. Details : ISO 9001 contains all of the requirements which an organisation must address within their Quality Management System (QMS) if they wish to be certified against the Standard. The majority of these requirements would be identified by many organizations as 'common sense' topics which they would want to address in order to run their business well e.g. sales, design, purchasing, training, calibration of test equipment, control of records. ISO 9001 is written by a committee (TC 176) and is designed for use in any type of organisation. This inevitably means that there are compromises in the wording of the Standard and some interpretation is often needed.

Achieve excellence with Legal Mind Business Solution's ISO certification service. We specialize in offering organizations flawless ISO certification solutions as a reputable brand in the sector. Our knowledgeable staff guarantees a quick and easy procedure and will walk you through all the requirements to become ISO certified. We customize our services to match your unique needs, whether you need certifications for ISO 9001, ISO 14001, ISO 27001, or other standards. At Legal Mind Business Solution, we take pleasure in offering first-rate client care, quick support, and affordable solutions. By collaborating with us, you can show that you are dedicated to excellence and quality by earning ISO certification. To take your company to new levels of success, get in touch with us right away. 

Our ISO Certification Service empowers businesses to achieve international standards, enhancing credibility and operational efficiency. We guide clients through the ISO certification process, covering quality management, environmental impact, information security, and more. Our comprehensive support includes documentation, audits, and compliance assessments, ensuring alignment with global benchmarks. Attaining ISO certification signifies a commitment to excellence, fostering customer trust and opening doors to new opportunities. Join us to elevate your business standards and demonstrate a dedication to quality on a global scale.

International Standard Organization is a world-renowned statutory body that provides Quality Control, Quality Assurance and Quality Management certifications. ISO Certification is kept in high regard as it testifies of an organization�s credibility. Other reasons to get an ISO Certification are mentioned as follows: Many customers only to do business with ISO Certified companies It provides competitive advantage Real issues highlighted when external views of trained auditors are provided Organizations are motivated to keep on improving their quality standards when ISO Certification audits are impending