The Association of Medical Research Charities (AMRC) have collated a variety of useful resources relevant to public engagement in research. Including training, involvement methods, payment guidance and supporting diversity.

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.

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.