NIHR (National Institute for Health and Care Research) has created a toolkit to support meaningful engagement with local communities in health and social care research.

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

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.