By Bhanvi Satija
LONDON, Oct 6 (Reuters) – AI-based medical devices will need constant monitoring even after they’re approved for use, rather than a single pre-approval safety check, the head of the UK’s medicines regulator said on Tuesday.
The UK government will accept all 44 recommendations from a report on how such AI tools are approved, it said.
• The government commits to publishing a full implementation plan by spring 2027, with a draft plan expected by the end of the year
• The plan will spell out delivery targets and timelines for putting each change into place across the NHS
• Britain is the first country to develop comprehensive rules for this emerging technology
• Lawrence Tallon, Medicines and Healthcare products Regulatory Agency Chief Executive, told Reuters many nations are now approaching the UK to learn from its approach
• “We’re moving into a much more sophisticated and complex era of AI as a medical device where we have non-deterministic algorithms,” he said, referring to AI systems that evolve and adapt while doctors are using them
• The MHRA will also start accepting applications for the third phase of its AI Airlock program, focusing on post-market surveillance and lifecycle monitoring after devices enter clinical practice
(Reporting by Bhanvi Satija, Editing by Rosalba O’Brien)
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