Much of the UK’s medical device and AI regulation remains under development and will presumably appear on the AI and Digital Regulations Service list in due course. Medical devices that are CE marked under the EU Medical Device Regulation (MDR) will be recognized in Great Britain until 30 July 2024, after which products must be Conformity Assessed (UKCA) marked.

In October, the MHRA announced its plans to introduce “legislatively light” AI regulation compared to the EU proposals for a heavy, horizontal regulation known as the AI Act.(Also see "MHRA Says UK Approach To AI Regulation ‘Legislatively Light’, Unlike EU Proposals" - Medtech Insight, 18 October, 2022.).

UK’s NHS Launches AI Regulation Service Specifically For Medtech Firms

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