DHF, DMR, DHR, Technical File and Design Dossier - Key Requirements and Future Directions - Webinar By GlobalCompliancePanel 2011

The 2011 Requirements and Future Directions webinar is dedicated to FDA and NB Audit Focus, Future Directions, Parallel Approaches to Documentation, TF / DD Expected Contents, DHF "Typical" Contents, Design Control vs. a Product `Snapshot in Time`, The EU`s MDD and the Technical File / Design Dossier and The U.S. FDA`s DHF.