U. S. FDA-regulated companies are responsible for understanding current Good Manufacturing Practices (CGMPs) as defined in the Code of Federal Regulations ( 21 CFR Part 111, 210/211, and 820).
Zero Defects and the CGMPs - Pros and Cons - Webinar By GlobalCompliancePanel
11 April 2012, Wilmington, United States
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OnlineTraining
OnlineTraining, 1000 N West Street,, Delaware, Suite 1200, Wilmington, 19801, United States
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