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
Venue
Online Training

Livermore Common, Online Training, Fremont, CA, 94539, United States

Organised by
GlobalCompliancePanel
Contact information
Search
 
 
Showing all upcoming events
Start Date
End Date
Location
Subject area
Event type

Advertisement
Spotlight


E-mail Enquiry
*
*
*
*