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.

The Public Engagement in Data Research Initiative (PEDRI) convened an online roundtable to explore how EDI can be strengthened across public involvement and engagement (PIE) in data research and statistics. This summary report outlines the discussion on opportunities and ongoing challenges in embedding EDI within data and statistics.

The National Centre for Population Health and Wellbeing Research provides a best practice guide to support researchers with co-production, along with three workshop reports that build on this guidance. These reports share work with young people to highlight research topics of importance.