Participant Information & Consent

The CHAANZ Registry operates under an Opt-Out Consent Process. If you are a person with Congenital Heart Disease, or you care for someone with Congenital Heart Disease, and you do not want to be included in the CHAANZ Registry, you can read through the study information and complete the Opt-Out consent form at the bottom of the page.

To access the study information and Opt-Out Consent form please select the link below that best describes you.