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  2. ISO 13485 - Wikipedia

    en.wikipedia.org/wiki/ISO_13485

    ISO 13485 Medical devices -- Quality management systems -- Requirements for regulatory purposes is a voluntary standard, [1] published by International Organization for Standardization (ISO) for the first time in 1996, and contains a comprehensive quality management system for the design and manufacture of medical devices.

  3. Quality management system - Wikipedia

    en.wikipedia.org/wiki/Quality_management_system

    ISO 9000:2005 provides information on the fundamentals and vocabulary used in quality management systems. ISO 9004:2009 provides guidance on a quality management approach for the sustained success of an organization. Neither of these standards can be used for certification purposes as they provide guidance, not requirements.

  4. Device Master Record - Wikipedia

    en.wikipedia.org/wiki/Device_Master_Record

    The sub-clause 4.2.3 of ISO 13485:2016 requires a manufacturer of medical device to establish a Technical file, similar to a device master record. The EU medical device regulation requires a manufacturer of a medical device to maintain a Technical documentation.

  5. Quality management - Wikipedia

    en.wikipedia.org/wiki/Quality_management

    These included those related to the production or processing of goods typically regulated by nations and other global jurisdictions, to ensure that unique elements pertaining to public health and safety are integrated into these Quality Management Systems. ISO 13485 specifies Quality Management System requirements for organizations involved in ...

  6. Medical device - Wikipedia

    en.wikipedia.org/wiki/Medical_device

    The ISO standards for medical devices are covered by ICS 11.100.20 and 11.040.01. [34] [35] The quality and risk management regarding the topic for regulatory purposes is convened by ISO 13485 and ISO 14971. ISO 13485:2016 is applicable to all providers and manufacturers of medical devices, components, contract services and distributors of ...

  7. ISO 9000 family - Wikipedia

    en.wikipedia.org/wiki/ISO_9000_family

    The ISO 9000 family is a set of international standards for quality management systems.It was developed in March 1987 by International Organization for Standardization.The goal of these standards is to help organizations ensure that they meet customer and other stakeholder needs within the statutory and regulatory requirements related to a product or service.

  8. List of ISO standards - Wikipedia

    en.wikipedia.org/wiki/List_of_ISO_standards

    Download as PDF; Printable version; In other projects Wikimedia Commons; Wikidata item; ... ISO 16000 – ISO 17999; ISO 18000 – ISO 19999; ISO 20000 – ISO 99999.

  9. International Organization for Standardization - Wikipedia

    en.wikipedia.org/wiki/International_Organization...

    The International Organization for Standardization (ISO / ˈ aɪ s oʊ /; [3] French: Organisation internationale de normalisation; Russian: Международная организация по стандартизации) is an independent, non-governmental, international standard development organization composed of representatives from the national standards organizations of member ...