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.

GRIPP2 provides guidance for reporting patient and public involvement in health and social care research.

National Co-ordinating Centre for Public Engagement (NCCPE) provides practical tools and content to help you develop your partnership approach and put it into practice.