DHF, DMR, DHR, Technical File and Design Dossier - Key Requirements and Future Directions 2015

28 Jul 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 - 28 Jul 2015, Webinar (51541)

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

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Health & Medicine: Medical device, Nutrition, Pharma

Science: Life Sciences & Biology

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