The Australian Government is undertaking a significant program of reform to the regulation of therapeutic goods in Australia. The reforms will continue to improve the safety, performance and quality of medical devices in Australia and improve health outcomes for patients who require medical devices. As part of the Australian Government Department of Health and Aged Care, the Therapeutic Goods Administration (TGA) regulates therapeutic goods, and is responsible for implementing the Government's reforms. The TGA has issued this consultation paper as part of the Government's reform program.
We invite you to review the third consultation paper and provide a response using our online survey, both of which are accessible through our TGA Consultation Hub. We appreciate all views, so if you would prefer to respond by email or written document, you can find further details on the hub.
This consultation will inform the policy decisions that will be made by the Australian Government.
For enquiries relating to the consultation document or your submission please email email@example.com.
The Department of Health and Aged Care acknowledges First Nations peoples as the Traditional Owners of Country throughout Australia, and their continuing connection to land, sea and community. We pay our respects to them and their cultures, and to all Elders both past and present.