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).

Organization

Country / Region

United Kingdom

License

Open Government Licence 2.0 (United Kingdom)

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