Patient and public input into the use of data in research is a priority for the BRC.

Key features include:

• Engagement activities focusing on interactive experiences aimed at demystifying the use of data in research
• Workshops and focus groups with local community groups to understand the concerns and wishes of people not normally involved in research
• Coproduction, by patients and the public working with researchers, of principles for the use of data in research at UCLH.

We also run a Citizens Data Network of people interested in inputting into the way data is used in research.