The New EU MDR PMS Requirements
NSF International presents a webinar on best adapting to the new EU MDR PMS requirements. This webinar provides practical steps for getting a return on investment by implementing feedback for risk management and usability engineering.
The webinar outlines how to avoid unnecessary duplication for post-market clinical follow-up by correctly aligning with PMS. It also covers how a PMS system interacts with other MDR requirements, and explains why the PMS requirements have been pushed into new European regulation.
Webinar Type: Recorded