The AI Airlock programme report contains a comprehensive overview of the methodology for establishing the regulatory sandbox, an overview of the seven case studies and the lessons learned from the independent programme evaluation. The report also summarises the key technical and regulatory insights and recommendations for changes to the regulatory and support framework for AI as a medical device.
Also included on this page is the detailed innovator case study reports. These have been drafted by the innovators and do not constitute MHRA guidance or policy.
Excerpt from the official page. The original is authoritative.