Conferences
Conference Details
US FDA Medical Device QSR, 21 CFR 820 and Quality Management System
Date :
Place : United States, San Jose
Contact Person:Ashutos Swain
Description:
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.US FDA Medical Device QSR, 21 CFR 820 and Quality Management System will be held in San Jose,United States on date 2021-06-08
Deadline for abstracts/proposals : 29th May 2021
Organized By :Complianceonline
Keynote Speakers :
Check the event website for more details.
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