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Guidance for reporting involvement of patients and the public (GRIPP2)

GRIPP2 provides guidance for reporting patient and public involvement in health and social care research.
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What do members of the public think about patient data?

Understanding Patient Data has compiled a summary of research and resources exploring public attitudes towards health data. Topics include trust in different organisations, opinions on decision-making, opt-out and choice, and how views differ among different groups of people.
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Can we create a culture of public engagement in data research?

A PEDRI (Public Engagement in Data Research) webinar exploring what creating a culture of public engagement means in practice to ensure that data research and statistics remains relevant, inclusive and impactful.
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