FDA Basic Intro Quality System Regulation

The presentation “Quality System Regulation 21 CFR 820 Basic Introduction” by Kimberly A. Trautman CDRH Medical Device Qualtiy System Expert at FDA is a brief overview of this central regulation for medical device manufacturers with some extra emphasis on Design Control elements. The full presentation is at the link provided.

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IEC 62304 and Emerging Standards Impacting Medical Device and HealthIT Software training course in Boise, Idaho. 3-Day course.

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