Webinar: Consent conversations

Thursday 30 May 2024 | 1.00PM-2.30PM AEST | Online | Free

Facilitator - Belinda Fazekas, National Project Officer, IMPACCT Trials Coordination Centre

In this webinar, we will explore the challenges of consent in a range of scenarios. The decision to participate in clinical research is the choice of each eligible person. This requires that they give informed consent, which should be voluntary and based on a clear understanding of the proposed research.

Face-to-face consent conversations between clinicians and patients are important. But, what happens to the consent conversation when the clinician and patient are in different locations? What are the challenges of consent for research that involves vulnerable people? What are the Good Clinical Practice (GCP) requirements for consent and how will this change when R3 is released?

We are pleased to introduce our program of speakers with expertise in consent.

Facilitator

Belinda Fazekas - Facilitator
National Project Officer
IMPACCT Trials Coordination Centre
University of Technology Sydney

Speakers

Dr Sophie Mepham
Group Executive Manager Oncology Research - Global
GCP Consultant
Presentation - GCP and Consent

Dr Anthony Herbert
Senior Lecturer
Children's Health Queensland Clinical Unit
University of Queensland
Presentation - Paediatric Consent

Professor Nikolajs Zeps
Adjunct Professor, Monash University, and
Director of Research, Northern Health
Presentation - eConsent as an enabler for participant engagement: practice examples for clinical trials and clinical quality registries

Dr Lisa Eckstein
Director, CT:IQ
University of Tasmania
Presentation - The CT:IQ InFORMed Project: Putting Participants at the Centre of Consent for Research

Don't miss out! Register today.

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