Call for evidence outcome

Equity in medical devices: independent review call for evidence

This call for evidence has closed

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Detail of outcome

We received submissions to this call for evidence from more than 50 respondents, who represented a broad range of stakeholders from across the UK.

These responses were considered and used to inform the final report of the independent review on equity in medical devices, which was published on 11 March 2024.

The response to this call for evidence includes:

  • a summary of all responses received and respondents
  • key themes that emerged from submissions
  • how insights from the call for evidence were used

Original call for evidence

Summary

We are seeking your views on the design, development, evaluation and use of medical devices.

This call for evidence ran from
to

Call for evidence description

One of the priorities for the UK government is to tackle health inequalities. As part of these efforts, the former Secretary of State for Health and Social Care, Sajid Javid, commissioned an independent review on equity in medical devices.

The independent review aims to establish where and how potential ethnic and other unfair biases may arise in the entire lifecycle of medical devices, and the extent and impact of these, and to make recommendations for more equitable solutions. To date the evidence is not yet conclusive.

See more information about the equity in medical devices: independent review.

The independent review is launching this call for evidence to collect existing data and evidence as well as information on ongoing data collection and research or evaluation projects. This call will be particularly relevant to those who engage in any way in the design, development, evaluation and use of medical devices.

Patients and members of the general public can also use the call to share their views and insights, but if patients have concerns about the health care received there are other dedicated channels and support available.

To provide feedback or complain about the care received to date, contact NHS England.

To report to the Medicines and Healthcare products Regulatory Agency (MHRA) suspected side effects to medicines, vaccines, e-cigarettes, medical device incidents, defective or falsified (fake) products, use Yellow Card.

Documents

Published 11 August 2022
Last updated 11 March 2024 + show all updates
  1. Added response to the call for evidence.

  2. Added contact email in case of any queries.

  3. First published.