The Patient Experience Library pulls together patient experience evidence from government bodies, health charities, patient voice organisations, academic institutions and more into evidence maps. These maps help researchers and research funders identify where the evidence base is saturated and where gaps remain.

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

This resource provides clarity on the definition of transparency and practical examples of its application in health data science to support public trust.