National Coordinating Centre for Public Engagement (NCCPE) lay out a set of principles and suggested actions to guide public engagement professionals to embed EDI into their work.

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.

A PEDRI (Public Engagement in Data Research) webinar exploring trauma‑informed public engagement in data research, focusing on empathy, safety and sensitive conversations.