Introduction

The U.S. FDA's DHF
The EU's MDD and the Technical File / Design Dossier
Design Control vs. a Product 'Snapshot in Time'
DHF "Typical" Contents
TF / DD Expected Contents
Parallel Approaches to Documentation -- Teams
Future Directions
FDA and NB Audit Focus

Useful links

• Further event details More information about the event

Venue

online training webinar

online training webinar, 1000 N West Street, Suite 1200, Wilmington, 19801, United States

Useful links

• Venue information More information about the venue

Organised by

global compliance panel