GMP Compliance for Quality Control and Contract Laboratories
October 19, 2018 - Online Event ON CAWebinar Compliance
info@webinarcompliance.com
Phone:416-915-4438\58
Quality control laboratories are considered high risk because after testing and approval pharmaceutical drug products and APIs are released to the market without further check. That’s the reason why FDA and other agencies put highest emphasis on inspections of QC laboratories. Even though cGMP regulations have been in place since long time, the large number of QC related 483’s and warning letters demonstrate that companies have problems with implementation.
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