Phone: 800-447-9407
RAPS Approved Webinar on
The DHF, DMR, DHR, and the Technical File-Design Dossier - USFDA and
EU MDD Requirements
Date: Wednesday, November 14, 2012 Time: 10:00 AM PDT | 01:00 PM EDT
Course "The DHF, DMR, DHR, and the Technical...
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Phone: 800-447-9407
RAPS Approved Webinar on
The DHF, DMR, DHR, and the Technical File-Design Dossier - USFDA and
EU MDD Requirements
Date: Wednesday, November 14, 2012 Time: 10:00 AM PDT | 01:00 PM EDT
Course "The DHF, DMR, DHR, and the Technical FileDesign Dossier - USFDA and EU MDD Requirements"
has been pre-approved by RAPS as eligible for up to
1.
5 credits towards a participant s RAC
recertification upon full completion.
Duration: 90 Minutes
Instructor: John E Lincoln
Location: Online
Price : $245.
00 (for one participant)
John E Lincoln
Consultant, Medical device
and Regulatory affairs,
Register Now
John E.
Lincoln is a medical device and regulatory affairs consultant.
He has helped companies to
implement or modify their GMP systems and procedures, product risk management, U.
S.
FDA responses.
.
.
.
more
Overview:
This webinar 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
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