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

  • 28 Jul 2015
  • Webinar

Description

DHF, DMR, DHR, Technical File and Design Dossier - Key Requirements and Future Directions 2015 is a webinar that covers topics such as:

  • 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

DHF, DMR, DHR, Technical File and Design Dossier - Key Requirements and Future Directions 2015 brings together QA, Senior management in Drugs, Devices, Biologics, Dietary Supplements, R&D, RA, Production, Engineering, Marketing and Operations.

Past Events

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: Medical device, Nutrition, Pharma
Science: Life Sciences & Biology

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