This webinar will greatly help device industry and relevant professionals understand how to define, document, implement, and maintain the procedures for MDR.
FDA-Compliant Medical Device Reporting (MDR) - Webinar By GlobalCompliancePanel
25 April 2013, Fremont, United States
Introduction
Venue
Online Training
Livermore Common, Online Training, California, Fremont, 94539, United States
Useful links
Organised by
GlobalCompliancePanel
Contact information
Mr John Robinson
1000 N West Street | Suite 1200, Wilmington, 19801, United States of America
8004479407
Contact us by email
1000 N West Street | Suite 1200, Wilmington, 19801, United States of America
8004479407
Contact us by email
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