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DHF, DMR, DHR, Technical File and Design Dossier - Key Requirements and Future Directions - Webinar by GlobalCompliancePanel

4 March 2014, Fremont, United States


Introduction
This webinar will examine the existing and proposed requirements for the FDA's DHF - including its derivative documents, the DMR and DHR.

It will consider the MDD's TF/DD requirements, and evaluate the documents' differing purposes / goals. Required and desirable contents will be discussed.
Venue
Online http://bit.ly/1k21EwF

Online http://bit.ly/1k21EwF, 161 Mission Falls Lane, Suite 216, Fremont, CA 94539, USA, Fremont, 94539, United States

Organised by
GlobalCompliancePanel
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