A repository of useful tools supporting secure data access. It contains diverse contributions from members of the International Population Data Linkage Network (IPDLN). The repository includes interactive data discovery tools, signposting support and good practice resources.

Connected by data share reflections on how to work well with public advisory panels.

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.