The DHF, DMR, DHR, and the Technical File-Design Dossier - USFDA and EU MDD Requirements - Webinar By GlobalCompliancePanel
The DHF, DMR, DHR, and the Technical File-Design Dossier - USFDA and EU MDD Requirements - Webinar By GlobalCompliancePanel

The DHF, DMR, DHR, and the Technical File-Design Dossier - USFDA and EU MDD Requirements - Webinar By GlobalCompliancePanel

Online Training · Wednesday, November 14, 2012 from 10:00 AM to 11:30 AM (Timezone: Pacific/Midway)

organizer
John Robinson
  • organizer
    John Robinson
Overview: This webinar will examine the existing and proposed requirements for the U.S. FDA's DHF - including its derivative documents, the DMR and DHR. It will consider the European Union's MDD TF/DD requirements, and evaluate the documents' differing purposes / goals, as well as the two different device classification schemes. Required and desirable contents will be discussed. Als... [read more]
Learn more: bit.ly/Ybg6G4
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