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.

This resource summarises public attitudes toward the use of patient data, based on research studies from 2010 to the present. It highlights key themes, such as support for using anonymised data for health research if there is public benefit, and concerns about industry using the data.

This webinar shares insights from a public contributor who talks about the importance of clear communication and provides tips for engaging the public effectively.