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Good patient and public involvement (PPI) means involving people affected by a health condition
and/or their carers in the various stages of a research proposal. This may include planning, designing,
implementing, managing, evaluating and/or disseminating their research. They are not just participants
in the research - they are actively involved in the decisions made about the research and are considered
part of the research team.
If you feel any of the information on this page needs amending or would like to request the deletion of this page, please contact us at publicpartnerships@nihr.ac.uk
