An online resource developed by the National Institute for Health and Care Research (NIHR) North West London Patient Safety Research Collaboration (PSRC) to help researchers navigate, improve and embrace public involvement.

GRIPP2 provides guidance for reporting patient and public involvement in health and social care 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.