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Total Documentation for Quality System Certification

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Quality Certification - ISO 9001:2015, ISO 13485, AS 9100

A Quality Management System (QMS) is collection of business processes that focused on customer requirements and their satisfaction. It is the much desired framework that is needed to monitor and improve performance in any specialized area of your business. It could improve the way your business operates or it could help you bring down your operating costs. It is set of policies, documented procedures and records that define how the company will operate in order to provide products and services to customers.

Benefits of Implementing Quality Management System with Our Documents

  • Our readymade Quality manual helps in Improvement of internal system of functioning.
  • Cost savings - decreases repeatative works.
  • Time saving - Readymade document templates helps in quick documentation.
  • It will guide in developing Quality Plan covering stage of inspections required.
  • Easy to validate implemented system via Quality audit checklists.
  • Quality Manual, quality procedures, quality plan, policy, forms, audit checklist, process flow charts etc. all the requirements covered inside documentation kit.

ISO 9001:2015 Certification

ISO 9001:2015 is internationally recognized world’s most popular Quality Management System Standard. ISO 9001:2015 Certification helps businesses and organizations to be more efficient and improve customer satisfaction. The ISO 9001:2015 certification doesn't certify products of the company. It only focuses upon working methodology that forces an organization to establish Quality Management System. This is generic standard can be deployed across all industries.


ISO 13485 Certification

A quality management system (QMS) designed especially for the medical device business must meet the standards of the worldwide standard ISO 13485 certification. It provides standards for businesses that create, develop, produce, install, and maintain medical equipment in order to guarantee adherence to legal requirements and client expectations. The achievement of ISO 13485 certification by an organisation signifies its dedication to upholding the most stringent standards of quality and safety in the manufacturing and dissemination of medical devices. Companies that comply with ISO 13485 are better able to control risks, produce higher-quality products, comply with regulations, and build customer trust.


AS9100 Certification

AS9100 is an international standard that applies quality management system requirement of Aerospace industry. AS 9100 Certification provides suppliers with a comprehensive quality system focused on areas directly impacting product safety and reliability in the aerospace industry. AS9100 standard gives you a set of guidelines to help make sure that you don’t miss any important elements so that your aerospace QMS can be successful.

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