Medical Device Complaint Handling: MDR, Reports of Removals and Corrections - Webinar by GlobalCompliancePanel

5 December 2013, Fremont, United States

Introduction

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.