Overview of the Quality System Regulation

U.S. Food and Drug Administration
U.S. Food and Drug Administration
17.1 هزار بار بازدید - 4 سال پیش - This CDRH Learn module discusses
This CDRH Learn module discusses the background, broad regulatory requirements and history of the FDA Quality System Regulation, 21 CFR 820 for medical devices.  The module defines key terminology used in the QS regulation, explains the purpose of a quality system, and explains the 7 major sub-systems approach.  To view more medical device educational resources please visit https://www.fda.gov/training-and-cont...
4 سال پیش در تاریخ 1399/09/25 منتشر شده است.
17,166 بـار بازدید شده
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