Through expert talks, workshops, and networking sessions, participants will gain valuable insights into the evolving EU regulatory landscape and how to ensure their technologies remain compliant. If you're navigating the complex world of medical device regulation, this is a must-attend event. Don’t miss it — registration is now open.

Hear the speakers discuss building your knowledge about MDR/IVDR requirements, gain insights from EC Representatives on the evolving EU regulatory environment, and participate in workshops and panel discussions.

Take a look at the programme here.

Find out all details about the event here.