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.
DHF, DMR, DHR, Technical File and Design Dossier - Key Requirements and Future Directions - Webinar By GlobalCompliancePanel
23 May 2012, Wilmington, United States
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Online Training, 1000 N West Street, Delaware, Suite 1200, Wilmington, 19801, United States
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GlobalCompliancePanel
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