MDR Module 7: MDR Exemptions

During MDR Exemptions, participants learn firsthand from the FDA how to navigate possible exemptions from some or all of the Medical Device Reporting requirements. A question and answer session takes place at the close of the main presentation.

Expert Faculty

William Huff
Public Health Analyst, 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)