The Association of Medical Research Charities (AMRC) have collated a variety of useful resources relevant to public engagement in research. Including training, involvement methods, payment guidance and supporting diversity.

DATAMIND share a variety of accessible resources about a project aimed at improving transparency, accessibility and engagement in longitudinal health research.

UK Health Data Research Alliance’s report provides recommendations for creating a data use register. A data use register is a public record showing how data is being used for research, who is using it and why. It helps show the value and benefits of using health data.