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.

This resource provides guidance on how to use accessible and simple language when talking about data to enhance communication with patients and the public.

This resource provides information to help guide researchers on planning, delivering, and evaluating public involvement activities, with tips, templates, and insights on participation and engagement.