Understanding Patient Data clarify the language of identifiability, explaining what it means to say that information has been through a process of anonymisation and the likelihood of re-identification.

National Co-ordinating Centre for Public Engagement (NCCPE) provides practical tools and content to help you develop your partnership approach and put it into practice.

Health Data Research UK (HDR UK) have created a 2-hour, self-paced training course that delves into why public trust is important in the context of clinical trials. Learn more about how to communicate and engage participants and the public on this topic on the HDR UK Futures platform.