This scoping review explores existing research on how the public has been involved in big data studies. It outlines different approaches to involvement and engagement, helping readers understand current practice and identify opportunities to strengthen public participation.

This PEDRI (Public Engagement in Data Research) webinar introduces using Equality Impact Assessments to embed equitable, inclusive public involvement in data research.

An online resource developed by the National Institute for Health and Care Research (NIHR) North West London Patient Safety Research Collaboration (PSRC) to help researchers navigate, improve and embrace public involvement.