A nationally informed, evidence-based resource designed to help health and medical research organisations embed meaningful consumer and community involvement (CCI) into their systems. Developed through extensive stakeholder engagement and implementation research, this guide covers ethical, policy, logistical, and structural considerations.
A clear, step-by-step guide for embedding meaningful consumer and community involvement into health and medical research systems. The Handbook is designed to be adaptable and user-friendly, encouraging organisations and individuals to tailor it to their specific context and needs. There are also dedicated resources for consumers on topics such as approaching an organisation and assessing […]
The toolkit provides practical advice for researchers and research organisations wishing to conduct patient-centred clinical trials. Using an interactive map, the Toolkit provides guidance and tools to help plan, deliver, evaluate and report consumer and community involvement and engagement activities. The Toolkit also contains a small but growing collection of dedicated resources for consumers and […]