ISO Certification Services

Type Of Service Provider Preferred Company   What you will gain:Higher Effectiveness and Efficiency on their JobExcellent Career Enhancement OpportunityInternationally Recognized QualificationPhoto-identity Card from ASCB(Europe) Ltd. - UKListing among an International list of Quality Professionals.Complete our Internal Auditor ISO 13485 Training Course, guarantee the highest quality standards and remove barriers to market for medical devices. Gain auditing skills to confidently guide your organization towards ISO 13485 accreditation – an essential standard for all medical device manufacturers. ISO 13485 outlines quality management system requirements for design, development, production and servicing of medical devices and related services. Get to grips with the entire internal auditing process, learn to plan audits, report on results and lead on follow up action. Additional Information: Item Code: 13485 Pay Mode Terms: L/C (Letter of Credit),T/T (Bank Transfer) Port of Dispatch: Anywhere

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. 

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.

What is ISO 9001:2015 Certification?ISO 9001:2015 is the latest revision of the ISO 9001 international standards that specifics requirements for a quality management system (QMS).  The requirements are specified within seven clauses: Context of the organization Leadership Planning Support Operation Performance evaluation Improvement Organizations will get certified to this standard in order to demonstrate their ability to consistently provide products and services that meet customer, statutory and regulatory requirements. Certification is granted by accredited certification bodies (registrars) that will audit an organization at planned intervals to confirm conformance to the ISO 9001:2015 standard.The standard can be applied to any organization. Its benefits include enhanced customer satisfaction, standardized processes, improved quality of products and services, and a culture of continuous improvement.Role of consultant Awareness Training to personnel on ISO 9001 Training on Internal Quality Auditor Documentation like SOP, Quality Manual Conducting Internal Audit Assisting organization throughout in the certification process   We provide ISO 9001 certification consultancy in all over India including cities like Delhi, Mumbai, Chennai, Kolkata, Bengaluru, Ahmedabad, Hyderabad, Patna, Kanpur, Lucknow, Allahabad, Noida, Faridabad, Gurgaon, Jaipur, Ajmer, Jodhpur, Kota, Udaipur, Vadodara, Surat, Rajkot, Silvassa, Vapi, Pune. Aurangabad, Nashik, Goa, Daman, Diu, Raipur, Bilaspur, Bhubaneshwar, Cuttack, Jamshedpur, Vishakhapatnam, Siliguri, Guwahati, Varanasi, Shillong, Coimbatore, Mysore, Chandigarh, Indore, Bhopal, Shimla, Jammu, Sri Nagar, Rudrapur, Haridwar, Gangtok.Overseas clients are in Singapore, Mauritius, Thailand, China, Fiji Island, Sri Lanka and NigeriaISO 9001:2015 specifies requirements for a quality management system when an organization: Needs to demonstrate its ability to consistently provide products and services that meet customer and applicable statutory and regulatory requirements, and Aims to enhance customer satisfaction through the effective application of the system, including processes for improvement of the system and the assurance of conformity to customer and applicable statutory and regulatory requirements. All the requirements of ISO 9001:2015 are generic and are intended to be applicable to any organization, regardless of its type or size, or the products and services it provides.

• 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 

An ISO 27001 certification helps you scale your quality of products & services according to industry-wide global specifications & process. With this compliance backing you, prospects can have better assurance while working with you, and that means more deals and more revenue.

ISO 22000:2018 This document specifies requirements for a food safety management system (FSMS) to enable an organization that is directly or indirectly involved in the food chain: a) to plan, implement, operate, maintain and update a FSMS providing products and services that are safe, in accordance with their intended use; b) to demonstrate compliance with applicable statutory and regulatory food safety requirements; c) to evaluate and assess mutually agreed customer food safety requirements and to demonstrate conformity with them; d) to effectively communicate food safety issues to interested parties within the food chain; e) to ensure that the organization conforms to its stated food safety policy; f) to demonstrate conformity to relevant interested parties; g) to seek certification or registration of its FSMS by an external organization, or make a self-assessment or self-declaration of conformity to this document. All requirements of this document are generic and are intended to be applicable to all organizations in the food chain, regardless of size and complexity. Organizations that are directly or indirectly involved include, but are not limited to, feed producers, animal food producers, harvesters of wild plants and animals, farmers, producers of ingredients, food manufacturers, retailers, and organizations providing food services, catering services, cleaning and sanitation services, transportation, storage and distribution services, suppliers of equipment, cleaning and disinfectants, packaging materials and other food contact materials. This document allows any organization, including small and/or less developed organizations (e.g. a small farm, a small packer-distributor, a small retail or food service outlet) to implement externally-developed elements in their FSMS. Internal and/or external resources can be used to meet the requirements of this document.ISO 22000 sets out the requirements for a food safety management system and can be certified to it. It maps out what an organization needs to do to demonstrate its ability to control food safety hazards in order to ensure that food is safe. It can be used by any organization regardless of its size or position in the food chain.ISO 22000 is a food safety management system by the International Organization for Standardization (ISO) which is outcome focused,[1] providing requirements for any organization in the food industry with objective to help to improve overall performance in food safety. These standards are intended to ensure safety in the global food supply chain. The standards involve the overall guidelines for food safety management and also focuses on traceability in the feed and food chain. Food safety[edit] Food safety refers to all those hazards, whether chronic or acute, that may make food injurious to the health of the consumer.[2]ISO 22000 standard[edit] ISO 22000 is the most popular voluntary food safety international standard in the food industry with 51,535 total number of sites (as per the ISO Survey 2022). The ISO 22000 family are international voluntary consensus standards which align to Good Standardization Practices (GSP)[3] and the World Trade Organization (WTO) Principles for the Development of International Standards.[4] Defining the requirements for a Food Safety Management System (FSMS) and incorporating the following elements which as defined as FSMS principles: system management prerequisite programs HACCP principles

The international ISO 50001 standard established the requirements and guidance for organizations to successfully develop, implement, maintain and continually improve an energy management system (EnMS). Conformance to this standard will ensure your organization energy performance is continually improving, energy efficiency and consumption are optimized and costs are decreased. ISO 50001 certification will increase your employees awareness and motivation toward a more efficient use of energy, document your energy performance improvement efforts and promote the positive branding of your organization.

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.

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 &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&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'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.

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.

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.

• 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 India.CIL provide ISO 17712 certification in India. CIL is an accredited certification in India. The International Standards Organization (ISO) establishes testing standards on a wide variety of products. ISO 17712 pertains to mechanical security seals, which are classified into 3 groups: • High Security Seals • Security Seals • Indicative Seals The standard is a copyrighted product of the International Standards Organization (ISO).  The information presented below is intended to provide seal consumers with a general understanding of the ISO 17712 standard. The information is a paraphrased summary of the key sections of the standard with a focus on the MINIMUM requirements for high security seals such as bolt seals, cable seals and barrier seals. High Security Seals These seals are designed to provide the most security. The most common high security seals are bolt seals (typically 7mm diameter or more), cable seals (typically 3.5mm diameter minimum) and barrier seals. These seals also serve as barriers since they require special tools (heavy duty bolt cutters, cable cutters or cutting wheels) to remove the seals. Typical applications include placing a bolt seal or cable seal in the hasp of the door latch. Other common practices are to wrap the keeper bars of a shipping container (or truck trailer) with a long cable seal or use a barrier seal (also known as a “keeper bar lock”). The Customs-Trade Partnership Against Terrorism (C-TPAT) is a joint effort between the United States government and businesses involved in importing goods into the United States. One of the C-TPAT guidelines is to use seals rated High Security for international shipments which cross borders. ISO 17712 Requirements for High Security Seals Section 4.2.1 – All high security seals must be permanently marked with the manufacturer name (or logo) and uniquely numbered Section 4.2.2 – All high security seals must be marked with an “H” to designate the high security classification. Section 4.4.1 – All high security seals shall be designed to mitigate tampering and leave evidence if tampered. The seal manufacturer will also certify in writing that they conduct periodic tamper evident testing on their seals in conjunction with an accredited process review organization. Section 5.1.2 – All high security seals must be tested by an independent testing lab to successfully pass minimum levels for tensile, shear, bending, and impact. Seals are tested as sold. The independent lab testing must be completed AT LEAST every 24 months to verify seals are still in compliance, or sooner if there is a significant design change in the seal. All of CIL’s high security seals meet the requirements for ISO 17712. The links to our certifications can be found on the respective product pages. Security Seals These are mid-level security devices which are lower cost than High Security Seals, but offer a higher break strength than Indicative Seals. The higher break strength assures the seals are durable for the application and not prone to breaking unintentionally. These seals typically include lower diameter cable seals (3mm diameter and less) and the high-strength plastic seals. These seals are typically removed with cable/wire cutters or other light weight tools. Indicative Seals These devices offer the lowest level of security. They are intended to show tampering, but are not intended to be a barrier for access. This category typically includes metal, plastic, or wire seals which can be pulled apart by hand or cut with a tin snips or scissors

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    

• 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.

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.

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.

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.

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.

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.

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

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.  

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

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.

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