National Co-ordinating Centre for Public Engagement (NCCPE) provides guidance and further resource on how to use evaluation to develop effective public engagement practice and to inform culture change.

This Health Data Research UK bite-sized video covers strategies to build trust and engage underserved communities in data-enabled clinical trials. You will discover how partnerships, co-design and addressing barriers to participation can foster inclusivity and improve diversity in trial participation.

The NIHR (National Institute for Health and Care Research) Innovation Observatory provides a framework to support researchers to involve public members in evidence syntheses (a process to summarise available evidence) with short time frames.