What is the Origin of Therapeutic Goods Administration (TGA)?

The TGA operates under the Australian Department of Health and was established to provide a unified, scientifically rigorous regulatory framework for therapeutic products. Its structure and function are similar to those of the FDA in the United States or the EMA in Europe, ensuring that products available to the public meet high standards of quality and are appropriately labeled with substantiated claims.

What is the Mechanism of Therapeutic Goods Administration (TGA)?

The TGA operates a multi-tiered regulatory mechanism that requires different levels of evidence depending on the product's risk and claims. Prescription medicines undergo rigorous evaluation for safety and efficacy, while complementary medicines are listed or registered based on their ingredients

Therapeutic Goods Administration (TGA) ∞ Area

Therapeutic Goods Administration (TGA)

Meaning

The Therapeutic Goods Administration, or TGA, is the regulatory body in Australia responsible for safeguarding the health and safety of the community by regulating the quality, safety, and efficacy of therapeutic goods. This includes prescription medicines, vaccines, medical devices, and a broad range of complementary medicines, many of which are relevant to the hormonal health and wellness space. TGA approval or listing is mandatory for all products legally supplied in Australia.