This Health Data Research UK bite-sized video explores the importance of trust in clinical trials that use healthcare data. It explains some of the reasons why trust varies across populations and its implications for promoting inclusivity in trial participation.

A PEDRI (Public Engagement in Data Research) webinar exploring what creating a culture of public engagement means in practice to ensure that data research and statistics remains relevant, inclusive and impactful.

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.