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About This Item

 

Full Description

This handbook is intended to guide organizations in the development, implementation and maintenance of their quality management system in accordance with ISO 13485. Organizations active in the medical device sector, such as manufacturers, importers, distributors, service providers certification bodies or regulatory bodies, can benefit from this publication.
 

Document History

  1. ISO 13485:2016 - Medical Devices - A Practical Guide, Advice from ISO/TC 210

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    ISO 13485:2016 - Medical Devices - A Practical Guide, Advice from ISO/TC 210

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  2. ISO 13485:2016


    Medical devices - A Practical Guide

    • Historical Version
  3. ISO 13485:2016 - Medical Devices - A Practical Guide


    Medical devices - A practical guide

    • Historical Version