Participant Information & Consent Form

Download the National PICF template featuring a tiered information framework:
Part A presents general information,
Part B contains study specific information with an informal letter style and;
Part C is the consent form with a formal tabular format.

Different projects and trials require different information.

To meet these needs we have prepared a range of supporting resources for researchers and participants.

Project Collaborators are representatives of wider stakeholders.

These included Industry partners, Regulatory and Peak Bodies, members of the Research and CRO community, Health sector sties, Consumer advocacy groups as well as Ethics and Governance representatives.

Can you make the PICF a more effective tool?

All comments and findings from the feedback page will be presented to the steering committee for review. The next steering committee will be held on the date below.