Therapeutic Goods Act 1989
In plain English
This Act regulates therapeutic goods, including medicines, medical devices, and accessories, to protect public health and safety.
The Therapeutic Goods Act 1989 regulates the import, manufacture, and supply of therapeutic goods. It applies to businesses involved in these activities. Businesses must meet standards for quality, safety, and efficacy. The Act came into force in 1989 and is regularly amended.
Why it matters
If your business deals with therapeutic goods, this Act is vital. Non-compliance can impact your business's ability to operate and affect consumer safety. Understand your obligations to avoid potential issues.
AI-assisted summary, grounded in the source link below. Generated 2026-05-23 via gemma3:12b.
Summary
TGA framework — ARTG, sponsor + manufacturer obligations, advertising code, post-market surveillance.
Topics
Administered by
Source: https://www.legislation.gov.au/Series/C2004A03808. Rules Mate summarises and links; we don't republish full statutory text. Always verify against the live source before acting.