This resource provides examples of effective public engagement in health data through case studies. It covers topics like public attitudes toward COVID-19 technology and using theatrical performance to engage wider audiences.

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.

The ODI offers a range of courses to help people build their data skills and improve data literacy. Some courses are free, while others require payment. Topics include data ethics, anonymisation and data protection, storytelling with data and more.