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.

Research Data Scotland (RDS) provide a simple explanation of how data is de-identified, what is meant by the term anonymisation and how this differs from pseudonymisation.

NEJM (New England Journal of Medicine) Evidence provides short animations that explain statistical concepts used in clinical research.