Watch Now

On-Demand Webinar

Medical device manufacturers distributing products in Europe have less than a year to comply with the European Medical Device Regulation.

To complicate matters, the requirement includes products already being distributed. For many manufacturers, there is still some uncertainty about what exactly needs to be done to comply and what data attributes need to be submitted to the EUDAMED. And, with more countries planning for their own unique device identification requirements, the challenges aren’t going away anytime soon. During this webinar, you will learn what steps you can take now to more easily comply with upcoming deadlines and future regulations.

The discussion will include:
 
  • Challenges medical device manufacturers are facing as they tackle EU MDR and IVDR compliance
  • Latest information on the technical specifications for the EUDAMED
  • Strategies for dealing with future global UDI regulations
  • Timeline for future UDI related regulations
  • Live Q & A

Date of Application
26 May 2020 MDR
26 May 2022 IVDR

About the Presenter:
Want our experts to work on your project?

Take the first step towards creating more value with USDM today.

Connect Now

We use cookies to understand how you use our site and improve your experience. This includes personalizing content and advertising. Learn more.