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Consumer advocacy is an approach where individuals with lived experience work to champion the rights, needs and priorities of the broader patient and carer community across healthcare, research and policy development. By doing so, consumer advocates can ensure that the lived experience perspective is embedded in decisions being made. Consumer advocates take on roles like […]
Consumer partnership is a collaborative approach where researchers, healthcare providers, and consumer organisations work together in a meaningful and active way to design and conduct research or healthcare improvement projects. These partnerships often involve broad collaboration between research teams and consumer organisations or groups, with one or more consumer partners helping to guide the direction […]
The Statement aims to guide research institutions, researchers, consumers and community members in the active involvement of consumers and community members in all aspects of health and medical research. It is under review in 2025. Appendix 3 of the Statement, ‘the research cycle’, helps researchers plan and implement meaningful consumer and community involvement across all […]
Advice on best practice consumer involvement in MRFF-funded health and medical research including principles for consumer involvement and implementation advice.
The Strategy is an implementation resource to strengthen partnerships between health policy makers and the community.
The standards provide a flexible framework for effective public involvement in research, promoting reflection, learning from both successes and failures, and supporting continuous improvement across diverse methods and contexts.
The Framework deepens understanding of trauma and its related concepts, offering guiding principles and outlining key domains to support trauma-informed approaches in everyday work.