DHF, DMR, DHR, Technical File and Design Dossier - Key Requirements and Future Directions 2015
12 May 2015
Webinar
Key Topics
The EU`s MDD and the Technical File / Design Dossier
The U.S. FDA`s DHF
DHF "Typical" Contents
Design Control vs. a Product `Snapshot in Time`
Parallel Approaches to Documentation -- Teams
TF / DD Expected Contents
FDA and NB Audit Focus
Future Directions
Who should Attend
QA, Senior management in Drugs, Devices, Biologics, Dietary Supplements, R&D, RA, Production, Engineering, Marketing and Operations.
Past Events
DHF, DMR, DHR, Technical File and Design Dossier - Key Requirements and Future Directions 2015 - 12 May 2015, Webinar (28426)
DHF, DMR, DHR, Technical File and Design Dossier - Key Requirements and Future Directions 2026
Important
Please, check "DHF, DMR, DHR, Technical File and Design Dossier - Key Requirements and Future Directions" official website for possible changes, before making any traveling arrangements
Event Categories
Health & Medicine: Healthcare, Medical device, Medical laboratories, Pharma
