MHRA Sets Out Summer Schedule Of Medtech Regulatory Milestones

Regulator and law firm broach new methods for lifecycle management of AI/ML devices

UK devices regulator signals near-term progress on PMS statutory instrument, policy statement on international recognition and input into IMDRF project to update  global diagnostics guidance.

AI Regulation
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Fresh back from the 25th session of the International Medical Device Regulators Forum (IMDRF) in March, the UK Medicines and Healthcare products Regulatory Agency hit the ground running in April to progress its ambitious regulatory system plans for Great Britain.

Government and policy schedules will be disrupted by the havoc of the UK’s 2024 general election, the date for which has yet to be nailed down. While the MHRA’s device Regulatory

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