AI sandbox to accelerate medicines development and improve medical device safety
MHRA has launched an AI sandbox to enhance medical device and medicine safety, speed up development processes, and reduce reliance on animal testing. This regulatory innovation supports faster evaluation of AI-enabled medical technologies.
🔖 Status: in-development
This reform is part of the MHRA's ongoing programme to modernise and strengthen the the UK medical device regulatory framework. Monitor the official source for updates on timelines, consultation opportunities, and implementation guidance. Where relevant, begin assessing potential impacts on your existing registrations, technical documentation, and compliance timelines so your organisation is prepared when the reform takes effect.
View official source ↗