Design History Files (DHF), Device Master Records (DMR), Device History Records (DHR), Technical Files , Design Dossiers - The Requirements - Webinar By GlobalCompliancePanel

6 March 2013, Fremont, CA, United States

Introduction

This webinar will examine the existing and proposed requirements for the U.S. FDA's DHF per the CGMPs, 21 CFR 820.30 (j) - including its derivative documents, the DMR and DHR.

Price: $245.00

GlobalCompliancePanel
Phone: 800-447-9407
webinars@globalcompliancepanel.com
http://bit.ly/Yatcnh