MD5: Post-market challenges

Richard Vincins

Richard Vincins outlined how post-market surveillance (PMS) is becoming increasingly important around the world in many jurisdictions. Previously, PMS activities used to be concentrated on vigilance and complaints, however the Medical Device Regulation (MDR) explicitly identifies sources of data which have not previously been properly identified or evaluated. Even if these are identified, the evaluation and analysis of their data was lacking in detail and methodology.

 This is member-only content

To read this article, SIGN IN NOW if you are a TOPRA member.

 

Not a TOPRA member yet? Join our global community.

Five great reasons to become a TOPRA member:

  1. Great savings on our events and training.
  2. Be part of our dynamic international community.
  3. Contribute to the profession.
  4. Grow your skills and knowledge.
  5. Take your career to the next level.

Have you heard what you’re missing? Listen now to the RegRapPod podcast show, for free!