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Rapid involvement of patients and the public in evidence synthesis (RIPPLES)

The NIHR (National Institute for Health and Care Research) Innovation Observatory provides a framework to support researchers to involve public members in evidence syntheses (a process to summarise available evidence) with short time frames.
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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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A Guide to Co-Producing Accessible Health Information

This guide helps public involvement and engagement professionals and researchers to collaborate with the public and patients, valuing their lived experiences to co-create easy to understand information. This ensures everyone equally grasps the benefit of health data.
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