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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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A framework for lived experience in applications and research

DATAMIND provide a framework  for including patients and the public  in  funding applications and research. From development, design and planning through to dissemination.
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Co-producing data research with under-served groups

This resource provides useful tips and practical guidance on how researchers can work collaboratively with people with lived experience to shape research projects through shared decision making and equal power.
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