The New EU MDR PMS Requirements Webinar

Manufacturers should expect to see a return on investment or “pay-off” when implementing the new EU MDR PMS requirements. This webinar provides practical steps for taking advantage by appropriately implementing feedback for Risk-Management as well as for Usability Engineering.

The webinar provides insights as how to avoid unnecessary duplication for Post-Market Clinical follow-up if correctly aligned with PMS. The webinar will also provide a perspective upon how a PMS system interacts with other MDR requirements and provides a rational as to why the PMS requirements have been pushed into new European regulation.