DHF, DMR, DHR, Technical File and Design Dossier – Key Requirements and Future Directions – Webinar By GlobalCompliancePanel
| May 23, 2012 |
Online Training
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. Read more »