MDR Module 4: Improving the Quality of Your MDR

Improving the Quality of Your MDR provides the FDA with a forum to share insight on how to complete the 3500A Form, and how to avoid common mistakes. Participants learn directly from the FDA on what not to do when filing an MDR. A Question and Answer session takes place at the close of the main presentation.

Expert Faculty

Linda Hoffman
Consumer Safety Officer, Office of Surveillance and Biometrics
Center for Devices and Radiological Health, FDA

(Expert faculty titles and companies may have changed since the time of recording.)



Learning Impact

Upon completion of this training, participants will:

  • Gain comprehensive knowledge of FDA expectations and guidelines
  • Learn industry standard definitions/applications
  • Gain insights and answers to audience-generated questions


$99 per module
$840 for entire series (Receive a 15% discount for purchasing all 10 modules)