Navigating the Medical Device Post-Market Maze and Challenges During COVID-19 Pandemic Online Seminar - Learn what FDA is Really Thinking on Regulation and Guidance Documents (May 13-14, 2021) March 10, 2021 05:33 ET | Source: Research and Markets Research and Markets Dublin, IRELAND ResearchAndMarkets.com's offering. Post-Market activities, Complaint Handling, MDRs, and Recalls are expensive, time-consuming, and often lead to more serious financial consequences. Over 80% of FDA Inspection target observations for lack of compliance in these areas. By attending this seminar, you will discover: How to overcome one of the biggest obstacles device manufacturers face How the FDA expects you to develop and implement proper handling of complaints reportable or non-reportable, product complaint handling, and documentation