This webinar will provide valuable guidance to regulated companies in development, implementation, or refinement of their manufacturing process verification and validation programs. It will evaluate validation practices that are more in agreement with ICH Q7 and Q8 than previously accepted validation methods, and will provide thought-provoking questions for FDA-regulated companies.
Process Verification and Validation to Meet U.S. FDA Requirements - Webinar By GlobalCompliancePanel
25 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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