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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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Equity, diversity and inclusion in public engagement
The University of Warwick provide guidance on what equity, diversity and inclusion is, why it is important in public engagement and tips on how to get started, as well as further resources.
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Patient Involvement Toolkit for Researchers
This resource provides information to help guide researchers on planning, delivering, and evaluating public involvement activities, with tips, templates, and insights on participation and engagement.
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