This presentation will step through the FDA regulations relating to post-market product problems, and give examples of how FDA currently interprets these regulations. Following this presentation, you should be able to decide whether your customer complaint requires not only investigation, but reporting to FDA, and in what format the report should be made, and to which section of the Agency.
Medical Device Complaint Handling: MDR, Reports of Removals and Corrections - Webinar by GlobalCompliancePanel
5 December 2013, Fremont, United States
Introduction
Venue
Online Training
Online Training, 161 Mission Falls Lane, Suite 216, California, Fremont, 94539, United States
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Organised by
GlobalCompliancePanel
Contact information
Mr John Robinson
161 Mission Falls Lane, Suite 216, Fremont, 94539, United States of America
8004479407
Contact us by email
161 Mission Falls Lane, Suite 216, Fremont, 94539, United States of America
8004479407
Contact us by email
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