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AI Regulation in the U.K. — New Government Approach (Updated) | Faegre Drinker Biddle & Reath LLP

In October 2022, the U.K. Medicines and Health products Regulatory Agency (MHRA) published its Guidance, Software and AI as a Medical Device Change Programme – Roadmap, setting out how...
United Kingdom Device Change Programme Faegre Drinker Biddle Reath International Medical Device Regulators Forum Regulatory Agency Faegre Drinker Biddle

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