TGA is the Therapeutic Goods Administration of Australia, a federal drug authority under the Ministry of Health of Australia, which ensures that Australian drugs meet applicable standards through a series of evaluation and supervision. The scope of its supervision includes pharmaceuticals, medical devices, blood and blood products.
According to the Australian Medical Products Act, all medical products (drugs and medical devices) listed in Australia must be registered or registered with the Australian Medical Products Authority (Australian Register of Therapeutic Goods, ARTG) after the product can be legally listed.