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MHRA outlines AI and MedTech...

The UK Medicines and Healthcare products Regulatory...

MHRA outlines AI and MedTech regulatory plans at AdvaMed 2026

The UK Medicines and Healthcare products Regulatory Agency (MHRA) outlined its evolving approach to artificial intelligence (AI) and medical device regulation at AdvaMed 2026, highlighting lifecycle-based oversight, regulatory sandboxes and closer cooperation with the US Food and Drug Administration (FDA). The plans build on the MHRA 2030 Strategy, published on 14 October 2026, and aim to support innovation while maintaining patient safety. MHRA 2030 strategy and centre for AI and Digital Health The MHRA’s 2030 Strategy set out plans to modernise regulation in response to advances in AI, personalised medicine and...
top-pharma -
Medical Devices

MHRA outlines AI...

The UK Medicines and Healthcare products Regulatory Agency (MHRA) outlined its evolving approach to artificial intelligence (AI) and medical device regulation at AdvaMed 2026,...
top-pharma -
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