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United States - Healthcare - The MHRA's "AI Airlock" – What Do You Need To Know?

In our blog post on 22 February 2024 we reported on the Medicines and Healthcare products Regulatory Agency (MHRA) announcement that it intended to launch a regulatory sandbox for software and AI medical devices called the "AI-Airlock".
United Kingdom Regulatory Agency Nhs Ai Lab Device Change Programme Department Of Health United Kingdom Approved
Source: mondaq.com

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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UK Government proposes a new approach to regulating artificial intelligence (AI) | Perspectives & Events

In July, the UK Government published a Policy Paper setting out the Government's vision for the future "pro-innovation" and "context-specific" AI regulatory regime in the UK. The Policy Paper outlines six cross-sectoral AI governance principles and confirms that the UK Government is not currently pl...
United Kingdom Device Change Programme Alan Turing Institute United Kingdom Government Office Healthcare Regulatory Authority European Commission

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