Understanding Patient Data has compiled a summary of research and resources exploring public attitudes towards health data. Topics include trust in different organisations, opinions on decision-making, opt-out and choice, and how views differ among different groups of people.

This resource provides detailed guidance on how to carry out public engagement within research including guiding principles, involvement methods and case studies.

National Coordinating Centre for Public Engagement (NCCPE) lay out a set of principles and suggested actions to guide public engagement professionals to embed EDI into their work.