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Guidance and tools for public involvement

The Association of Medical Research Charities (AMRC) have collated a variety of useful resources relevant to public engagement in research. Including training, involvement methods, payment guidance and supporting diversity.
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Report – Children’s social care and homelessness in Northern Ireland: Connecting data, changing futures

ADR (Administrative Data Research) Northern Ireland, VOYPIC (Voice of Young People in Care have co-produced a report with care-experienced young people to showcase the value of administrative data for understanding the relationship between children’s social care contact and homelessness risk in Northern Ireland.
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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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