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Guidance on Involving the Public in Health Data Research

This resource provides best practices on fair and effective public involvement in health data research.
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A starting guide to Equity, Diversity and Inclusion (EDI) for public engagement professionals

National Coordinating Centre for Public Engagement (NCCPE) lay out a set of principles and suggested actions to guide public engagement professionals to embed EDI into their work.
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What are the best words to use when talking about data?

This resource provides guidance on how to use accessible and simple language when talking about data to enhance communication with patients and the public.
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