Date: 04 November 2021
Time: 09:00 -10:00 (UK time) and 16:00 - 17:00 (UK time)
What’s the webinar about?
The Medical Device Regulation (MDR) is fully applicable in the EU since 26 May 2021. The timelines for ensuring your product achieves or maintains EU market access under the new, more stringent MDR are challenging. Our webinar will provide you with useful information around the routes to conformity for personalised medical devices under the MDR.
Who should attend the webinar?
This webinar will be useful to manufacturers of personalised medical devices and anyone with an interest in the regulatory paths for personalised medical devices. Also, anyone who is involved with classification of personalised medical devices, will also find this webinar insightful.
What will participants gain?
Join Dr Tim Marriott, Senior Technical Specialist and Scheme Manager, BSI, to hear about important insights into routes to conformity for personalised medical devices. Tim will also be joined by Judith Prevoo, Regulatory Lead, BSI. Participants will gain an understanding of the regulatory requirements for personalised medical devices as well as an explanation of common pitfalls of classifying personalised devices.