Design History Files and Technical Files/Design Dossiers - Meeting U.S. FDA CGMPS and the EU's MDD Requirements

6 November 2013, Palo Alto, United States


Introduction
This 90-minute webinar will examine in detail the U.S. FDA and EU MDD requirements for DHFs, DMRs, DHRs, and TF/DDs - their formats, content, and their commonalities, differences, interrelationships, and similarities.
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ComplianceOnline
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Online Event, 2600 E. Bayshore Road, California, Palo Alto, 94303, United States

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