PRE-RECORDED WEBINAR: Understanding the Transition from MDD to MDR Next

PRE-RECORDED WEBINAR: Understanding the Transition from MDD to MDR

By Linda Chatwin

Time To Read Less than a minute

The new EU Medical Device Regulation (MDR) is over 300 pages long and incorporates major changes from the current regulatory system. In this webinar recording, Linda Chatwin shares her knowledge on the new Medical Devices Regulation and tips on how to prepare for the transition from the EU Medical Devices Directive (MDR).

This webinar covers the following:

  • Overview of the MDR
  • Understanding Transitioning from the MDD to the MDR
  • Notified Body Requirements
  • Interactions with Notified Bodies
  • UDI
  • Impact on CE Certifications

In this one-hour webinar recording, you get the advantage of seeing both the slides and the presenter.

Please fill out the form to get a link to the webinar:

Presenter: Linda Chatwin RAC JD, UL Medical Senior Customer Solutions Consultant

Ms. Chatwin has been involved with regulated medical products for over 30 years. She understands the regulatory maze required to bring products to market. She holds a Regulatory Affairs Certification and is holds a Juris Doctor degree. She has obtained product approvals for a wide range of products, and remains involved in changing requirements for medical devices worldwide. Currently, she heads the North American Advisory Services group for UL, LLC, assisting clients with regulatory issues and challenges, including implementation of UDI processes. Ms. Chatwin travels worldwide to speak about changing market access issues.