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Mapping patient experiences

The Patient Experience Library pulls together patient experience evidence from government bodies, health charities, patient voice organisations, academic institutions and more into evidence maps. These maps help researchers and research funders identify where the evidence base is saturated and where gaps remain.
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Co-producing data-intensive research with an underserved group

This article from Administrative Data Research Centre Northern Ireland, explores how researchers and care-experienced young people worked together as equal partners to shape a data-driven research project. It aims to show what co-production looks like in practice, why it matters, and what helps or hinders success.
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Guidance on Involving the Public in Health Data Research

This resource provides best practices on fair and effective public involvement in health data research.
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