For information on accessing rapid antigen tests and what to do if you test positive, go to COVID-19 testing on the Department of Health website.
We conduct public consultations as part of our broader stakeholder engagement work, including on changes to regulatory requirements or practices, reviews of business processes, standards or guidelines, and TGA fees and charges.
Closed on 12 January 2018
Medicines and Medical Devices Regulation Review
The Therapeutic Goods Administration is part of the Health Products Regulation Group