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