US FDA Medical Device QSR, 21 CFR 820 and Quality Management System
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Learn the basic overview of the original medical device Quality Management System -- The US FDA’s CGMP, Quality System Regulation (QSR) under 21 CFR 820. Implementation, training requirements and content, and annual internal audit / inspection expectations. The FDA’s four key areas of compliance under QSIT.
Details
Costs: $199
Event type: Seminars, workshops and presentations
Registration information: n/a
Posted by: Ashutos Swain
Organizer
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