Redesigning Consent to Research: Putting Patients and Participants at the Centre

About the Event

At this inaugural webinar of CT:IQ, you’ll join a panel of experts as they explore the pathways forward in Australia to promote participant-centered consent to research.

CT:IQ partnered with the ARDC Health Studies Australian National Data Asset (HeSANDA) program to develop a National Data Sharing Statement. Learn more about this project.

Topics

• The ethical and legal role of Participant Information Sheets and Consent Forms (PICFs)
• Designing PICFs with patients and participants at the centre
• Moving forward with participant-centred research in Australia

Do you have questions about this event? Contact CT:IQ.