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

The Office for National Statistics (ONS) have created a toolkit of communication resources to help increase the public’s understanding of how data and statistics are used to benefit local communities.

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.