Basic Documentation Requirements for Compliance under U.S. FDA and EU MDD

MessageThis Webinar is over
Date Mar 28, 2017
Time 01:00 PM - 02:30 PM
Cost $227.00
Online

Product Format: Live Webinar
Presenter(s): John E. Lincoln 
Conference Date:  Tue, Mar 28, 2017
Aired Time: 1 pm ET | 12 pm CT | 11 am MT | 10 am PT
Length: 90 minutes
Price: $227.00
 
This webinar by expert speaker John E. Lincoln will examine the existing and proposed requirements for the U.S. FDA's DHF - including its derivative documents, the DMR and DHR. It will consider the European Union's MDD TF/DD requirements, and evaluate the documents' differing purposes/goals, as well as the two different device classification schemes.
 
For Registration, visit https://www.audioeducator.com/pharma-biotech/us-fda-eu-medical-device-eirective-requirements.html  
 
Special Offer: Use code EVENT25 to get $25 discount.
 
Not able to attend the audio session? We will provide you with a replay of the session, or you can request a DVD recording.
 
For any queries feel free to contact Customer Service at 1-866-458-2965 or e-mail at customerservice@audioeducator.com.

 


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