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What do we mean by public benefit? (2022)

The National Data Guardian for Health and Social Care in England provides guidance on the concept of ‘public benefit’ in the context of data sharing, informed by a formal dialogue with the public.
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Rapid involvement of patients and the public in evidence synthesis (RIPPLES)

The NIHR (National Institute for Health and Care Research) Innovation Observatory provides a framework to support researchers to involve public members in evidence syntheses (a process to summarise available evidence) with short time frames.
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Resources for public involvement with AI (Artificial Intelligence) to understand multiple long-term conditions

A collection of resources focused on public involvement in data research, compiled by the AI for Multiple Long Term Conditions Research Support Facility (AIM RSF) at the Alan Turing Institute.
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