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.

National Co-ordinating Centre for Public Engagement (NCCPE) provides practical tools and content to help you develop your partnership approach and put it into practice.

This webinar by the British Heart Foundation Data Science Centre offers guidance on working with communication and public relations teams to reach diverse groups and highlights how effective dissemination can have an impact on policy.