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2-day In-person Seminar (July 9-10, 2015)

GMP Boot-Camp: Understanding FDA’s GMP Requirements for Pharmaceuticals


Location: Philadelphia PA

Overview:

This workshop will present the current regulations, guidance documents and regulatory strategies available for manufacturing pharmaceutical products. Case studies and examples will be used to highlight key areas of compliance, common errors identified by FDA, and trends in the industry. Perspectives for different classes of products will be used to emphasize general and the product specific issues.  


For additional information on the workshop agenda and logistics, please call 410-501-5777 or email: info@fdamap.com
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FDA’s  GMP Expectations for Phase I and First-in-Man Clinical Trials

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