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.
RELATED RESOURCES
Senate Inquiry Submission – menopause and perimenopause
24 May 2024,
COTA Submissions
Joint Submission – Aged Care Act Exposure Draft
12 March 2024,
COTA Submissions