The National Institute for Health and Care Research (NIHR) Policy Research Unit in Maternal and Neonatal Health and Care (PRU-MNHC) share key themes identified from their research project, to support researchers to engage and involve people who are currently under-represented in health research.

This toolkit from the Office for Statistics Regulation (OSR) supports statistics producers to involve and engage the public in statistic production.

This article shares findings from the PIONEER Health Data Research Hub at Health Data Research UK. The team engaged 350 patients, carers, healthcare staff, and public members to explore their views on how anonymised health data is used for research and their awareness of the NHS data opt-out.