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What does my health data look like and how is it used?

A playlist of videos from Use My Data where experts speak about a variety of topics to help patients and the public understand what their data looks like, how it can be used to measure inequality, explain statistical terms used in healthcare and more.
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Research Cycle: Engaging Patients and the Public

This infographic provides an overview of the research cycle and highlights opportunities for public and patient involvement at every stage of the research process.
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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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