Different types of medicines are regulated in different ways by the Therapeutic Goods Administration (TGA), depending on what they contain and how they are to be used. The level of regulatory scrutiny increases with the level of risk the medicine can pose to consumers. This approach allows resources to be targeted effectively.
23 September 2021, COTA Submissions
8 September 2021, COTA Submissions
6 August 2021, COTA Submissions