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 resource provides best practices on fair and effective public involvement in health data research.

A practical planner and tracker created by Cardiff University to support the integration, impact assessment and reporting of public involvement in research.