UK regulator adopts AI framework for medical devices, launches next phase of AI sandbox
The Medicines and Healthcare products Regulatory Agency announced that the UK government has accepted a set of recommendations on using artificial intelligence in medical devices. These recommendations were developed by an independent group of NHS doctors.
The agency said the adopted framework will guide how AI-based medical products are evaluated and brought to market, aiming to ensure safety and effectiveness while fostering innovation.
In addition, the MHRA is starting the third phase of its AI Airlock, a regulatory sandbox that allows developers to test new AI technologies under supervision before wider deployment.
This writeup was produced by pharmadog from original reporting by raps.
Original headline: “MHRA adopts AI framework proposed by UK docs”
read at raps ↗
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