The MHRA recently launched its public consultation on the future regulation of medical devices in the UK. The consultation is open until the 25th of November and the timeline is definitely tight for stakeholders to provide views.
In this Lexology hosted webinar, our Alex Denoon and Xisca Borrás take an in-depth look at all of the published proposals and consider how these are likely to impact the UK's medical devices framework and industry.
This comprehensive overview will be useful to all those who want to be brought up-to-date with the proposed regulation, and especially the companies and individuals who wish to respond to the consultation.
Note: all information in the video was correct as of the time of recording - 6 October 2021
For more information on the work we do, check out our life sciences regulatory practice.
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