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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
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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- Most Recent
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ISO 13485:2016
Medical devices - A Practical Guide- Historical Version
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ISO 13485:2016 - Medical Devices - A Practical Guide
Medical devices - A practical guide- Historical Version