Resources
PACT's working documents, guidelines, and training materials, for research teams, partners, patients, and the public.
The principles, standards, and agreements under which the PACT Lab operates.
Governing document
The principles and rationale underpinning the PACT Lab's approach to patient and public involvement.
Coming soon
Guidance
Practical standards and procedures for involving patients and the public in research responsibly and consistently.
Coming soon
Materials for researchers seeking certification, and for patients, caregivers, and members of the public taking part in research.
Training
Modules covering when and how to involve patients and the public, what counts as meaningful involvement, and how to budget for it.
In development
Training
A tiered pathway: self-advocacy and navigating the health system, then representing others with the same condition, then formal advocacy roles.
In development
How to request the PACT Lab's support and what to expect.
Service information
What the Lab can support now, what follows in the first year, and what follows in the second, with guidance on requesting support and costing involvement into grants.
Method
Collective Reflective Equilibrium in Practice: how public input is taken from data to defensible policy and translation recommendations.
Mapping
Which involvement resources exist across the two institutions, who manages them, and how access is decided.
Public panel
A demographically representative public panel of over 4,000 members, and how research teams can request access to it.