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US FDA Medical Device QSR, 21 CFR 820 and Quality Management System 2025
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(0 reviews)Tuesday, June 8, 2021 (1 day), San Jose, United States
Overview
Date: Jun 8, 2021 (1 day)
Venue online event, San Jose, United States
Organizer ComplianceOnline
Expected number of attendees : 1
Expected number of exhibitors : 1
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.
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