This guide helps public involvement and engagement professionals and researchers to collaborate with the public and patients, valuing their lived experiences to co-create easy to understand information. This ensures everyone equally grasps the benefit of health data.

An online resource developed by the National Institute for Health and Care Research (NIHR) North West London Patient Safety Research Collaboration (PSRC) to help researchers navigate, improve and embrace public involvement.

DATAMIND share a co-created checklist to guide researchers on using data responsibly in mental health research.