Intertek's Assurance in Action Podcast Network podcast

Navigating the Medical Device Regulation (MDR) Transition

0:00
15:56
Rewind 15 seconds
Fast Forward 15 seconds

In this episode, we're counting down to a shift in the medical device industry: the transition from the Medical Device Directive (MDD) to the Medical Device Regulation (MDR). Our expert, Curtis Riley, Head of Notified Body at Intertek Medical Notified Body – Business Assurance, discusses the main challenges for manufacturers, explains the key differences between MDR and MDD, reviews the MDR timeline, and walks through the next steps for the MDR application process. Tune in to gain valuable insights into navigating the evolving landscape of medical device regulation.

Follow us on- Intertek's Assurance In Action || Twitter || LinkedIn.

More episodes from "Intertek's Assurance in Action Podcast Network"