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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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How Do People Feel About the Use of Data?

This resource summarises public attitudes toward the use of patient data, based on research studies from 2010 to the present. It highlights key themes, such as support for using anonymised data for health research if there is public benefit, and concerns about industry using the data.
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Public member recruitment guide

DARE UK (Data and Analytics Research Environments UK) has created a guide outlining good practice for recruiting public members to groups and activities.
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