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
Useful links
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
Related events
New Zealand Institute of 91AV Conference 2024 (NZIC-24)
24 November 2024 14:00 - 28 November 2024 14:00, Dunedin, New Zealand
Drugging the Multimorbidity Associated with Ageing
17 January 2025 09:30-17:00, London, United Kingdom
Future Labs Live Basel
27 May 2025 09:00 - 28 May 2025 17:00, Basel, Switzerland
European Glycoscience Community Webinar Series
25 January 2024 15:00 - 19 December 2024 18:00
Search
Advertisement
Spotlight
Explore
Membership
