Open call for evidence

Regulation of AI in Healthcare

Summary

The MHRA is seeking evidence on the regulation of AI in healthcare to inform the recommendations of the National Commission into the Regulation of AI in Healthcare.

This call for evidence closes at

Call for evidence description

Introduction to the National Commission into the Regulation of AI in Healthcare

The UK government wants to create a healthcare system that is fit for the future, using artificial intelligence (AI) to help improve care. To support this, new proposals are being considered for regulating medical devices that use AI.

AI has the potential to make healthcare safer, faster, and more personalised. It could help NHS staff work more efficiently and support the growth of health technology companies in the UK. However, AI also brings new challenges for how we regulate and oversee these technologies.

The MHRA, as the regulator for medicines, medical devices, and blood products, is continuing to consider what the regulatory rules should be for AI as a medical device. We have established the National Commission into the Regulation of AI in Healthcare to support this goal.

The National Commission brings together experts from technology, healthcare, law, patient groups, the public, government, and the NHS. The National Commission will tackle the most important questions about how AI should be regulated and to give recommendations to the MHRA, which will be published in 2026.

The Commission is chaired by Professor Alastair Denniston; with the England Patient Safety Commissioner Professor Henrietta Hughes as deputy chair.

The Commission and its four Working Groups includes leading health professionals, regulators, AI specialists and experts from across England, Scotland, Wales, and Northern Ireland.

There is a research and engagement programme, supported by the MHRA and Health Foundation, to ensure that patients’ and service users’ views are central to the Commission’s work.

About the Call for Evidence

To make sure the Commission hears from a wide range of people, this Call for Evidence invites contributions from people and organisations across the UK and internationally. The information gathered will help inform the Commission’s recommendations and help address key challenges in regulating AI in healthcare.

Other opportunities such as workshops are also planned to hear directly from patients and members of the public.

Anyone can take part, but we especially want to hear from:

  • Patients, the public, and charities
  • AI health tech companies and industry groups
  • NHS and independent healthcare leaders and health and care professionals
  • Healthcare provider organisations and professional bodies
  • UK and international healthcare regulators

Topics considered in the Call for Evidence

The Call for Evidence invites evidence and views on:

  • whether the UK’s framework for regulating AI in healthcare is sufficient
  • how the UK’s regulatory framework may need to be improved to ensure fast access to safe and effective AI medical devices
  • approaches to checking safety once AI medical devices are in use
  • how responsibility and liability are managed between different parties involved in the deployment of AI medical devices.

Your views

We would value any views and experiences that are relevant to you or your organisation. To support organisations who wish to further promote the Call for Evidence, we have produced digital posters that can be used in healthcare settings.

Please complete the questionnaire by 23:59pm (UK time) on Monday 2 February 2026.

If you have an enquiry relating to the policy content of the Call for Evidence, you can contact the MHRA by email at info@mhra.gov.uk with the subject line “National Commission into the Regulation of AI in Healthcare”.

The results of the Call for Evidence and the response will be published on GOV.UK following analysis of the responses.

Assistive technologies

If you use assistive technology (such as a screen reader) and need a version of this document in a more accessible format, please email webupdates@mhra.gov.uk using the subject line “National Commission into the Regulation of AI in Healthcare”. Please tell us what format you need, and which assistive technology you use.

Documents

MHRA: Regulation of AI in Healthcare - information and questions

Request an accessible format.
If you use assistive technology (such as a screen reader) and need a version of this document in a more accessible format, please email webupdates@mhra.gov.uk. Please tell us what format you need. It will help us if you say what assistive technology you use.

Ways to respond

or

Email to:

engagement@mhra.gov.uk

Write to:

National Commission into the Regulation of AI in Healthcare
C/o PPSE Team
MHRA
10 South Colonnade
Canary Wharf
London E14 4PU

Updates to this page

Published 18 December 2025

Sign up for emails or print this page