21 CFR Part 820: Medical Devices

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Quality System Regulation (formerly known as Current Good Manufacturing Practice (cGMP) for Medical Devices and in Vitro Diagnostic Products)

The Medical Devices mini-handbook is used in association with several ISPE training courses:

Attendees of the training course receive a complimentary copy of this publication.

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Bound Version $5 / €4 $5 / €4 buy now
Last Update: 18 June 2013

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