Software and AI as a Medical Device Change Programme
Information
Type
Guidance
Regulated products
Medical Devices
Topics
Health And Social Care
Published
September 16, 2021
Last updated
June 14, 2023
Description
The Medicines and Healthcare products Regulatory Agency (MHRA) have embarked upon an ambitious programme of reform to ensure that medical device regulation is fit for purpose for software, including artificial intelligence (AI).
Tags
Organization
Country / Region
United Kingdom
License
Open Government Licence 2.0 (United Kingdom)