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.Deadline for abstracts/proposals : 29th May 2021
Organized By :Complianceonline
Keynote Speakers :
Check the event website for more details.