The National Commission into the Regulation of AI in Healthcare argues the UK should shift away from one‑and‑done approvals for AI models. Instead, new systems would start in carefully supervised deployment with ongoing checks, graduating to full authorization only after they prove they are safe and effective in day‑to‑day care.
The panel calls AI‑enabled medical tools a major opening for the UK and says access needs to speed up, but not at the expense of safety or fairness. Regulators around the world are wrestling with how to judge AI‑infused health products, from AI that drafts clinical notes to imaging read by algorithms to wearables that track a person's health. These tools can sharpen accuracy and accelerate care, yet questions about safety and bias still loom.
The independent commission was launched by the Medicines and Healthcare products Regulatory Agency last September, and its report followed a consultation that reached roughly 12,000 people. Alastair Denniston, who chairs the commission and is a University of Birmingham professor in regulatory science and innovation, said AI is likely to sit among the most transformative advances in medicine, mentioned alongside antibiotics and X‑rays. "But as with any powerful technology, we need to understand how to use it safely," he said, warning that if progress is not made quickly the UK could miss out, or see tools put into use before they are ready.
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The report says patients should be able to easily find safety details about AI devices, and it recommends giving the MHRA tougher enforcement powers. Lawrence Tallon, the MHRA's chief executive officer, said the current system has served first‑generation AI tools, but this is a new era. "We need to reinvent the regulatory framework for the age of generative AI." He expects the MHRA to move quickly on regulations, while the government considers its formal response.
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