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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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Increasing equity, diversity and inclusion in patient and public involvement
The National Institute for Health and Care Research (NIHR) Policy Research Unit in Maternal and Neonatal Health and Care (PRU-MNHC) share key themes identified from their research project, to support researchers to engage and involve people who are currently under-represented in health research.
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Secure Data Environments explained
Understanding Patient Data explain secure data environments, their benefits and drawback, and examples of their use, as well as an animation.
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