This resource provides information to help guide researchers on planning, delivering, and evaluating public involvement activities, with tips, templates, and insights on participation and engagement.

This guide by National Co-ordinating Centre for Public Engagement (NCCPE) helps you take a strategic approach to building support for public engagement in your institution.

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.