Resources and guidance
Access regulatory guidance for industry, alongside tailored information for consumers and health professionals.
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For consumers
Learn how to safely access and use different health products in Australia.
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Travelling with medicines and medical devices
Whether you're leaving Australia for a holiday or coming to Australia to see the sights, it's recommended that you take your medicines or medical devices with you. -
Vapes: information for individuals and patients
Find out about therapeutic vapes for smoking cessation and the management of nicotine dependence, how they are regulated, and how they can be accessed. -
Medicine shortages: information for consumers
Understand medicine shortages and what to do if your medicine is affected.
For industry
Understand your obligations and access resources to support your work.
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Guidance
Our Guidance explains the laws and regulations governing the development, manufacturing, marketing, and supply of therapeutic goods in Australia. -
Australian Regulatory Guidelines (ARGs)
The ARGs group together resources about regulatory requirements for biologicals, medical devices and medicines. -
For health professionals
Access product information and safety updates to support your practice.
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Vapes: information for prescribers
Learn about the regulatory framework for prescribing therapeutic vapes for smoking cessation or the management of nicotine dependence. -
Safety updates
Refer to our articles for health professionals about health products and emerging safety issues. -
Medicine shortages: information for health professionals
General medicine shortage information and what to do if your patient’s medicine is in shortage.
Alerts
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Safety alerts
Refer to the latest safety alerts for medicines or medical devices with possible risks. -
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How to make a report
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Report a medicine or vaccine defect
Use this form to report defects that you think have arisen during manufacture, storage or handling of a medicine or vaccine. -
Reporting adverse events for consumers
How to report a side effect, reaction or other problem with a therapeutic good. Your report can help keep others safe. -
Reporting medical device incidents for sponsors and manufacturers
Industry portal - Log in to report medical device incidents via the Medical Device Incident Reporting (MDIR) system. -
Report a perceived breach or questionable practices
Use this form to report a perceived breach of the Therapeutic Goods Act, counterfeit products or questionable practices in relation to therapeutic products.
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Report non-compliant advertising
Use this portal to report a non-compliant advertisement for a medicine, medical device or any other type of therapeutic good.
Key resources
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Legislation
Find listed information for the legislation that is referred to in our Guidance content. -
Guidance
Our Guidance explains the laws and regulations governing the development, manufacturing, marketing, and supply of therapeutic goods in Australia. -
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Decision trees
Use decision trees to check rules for therapeutic goods in Australia, including classification, reporting obligations, advertising requirements and supply pathways. -
Resources
Search our resources for checklists, user guides, international scientific guidelines, compositional guidelines and forms.
Latest articles
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Prime Medic Group issued infringement notices for alleged unlawful advertising of weight loss medicines
Media releasesTGA has issued infringement notices to Prime Medic Group Pty Ltd (Prime Medic) and an individual for the alleged unlawful advertising of weight loss medicines in contravention of the Therapeutic Goods Act 1989 (the Act). -
TGA issues infringement notices to 6 individuals for alleged importation and unlawful advertising of therapeutic goods
Media releasesWe have issued 11 infringement notices totalling $43,560, to 6 individuals, for the alleged importation and unlawful advertising of therapeutic goods. -
Nitrosamine impurities acceptable intakes update - January 2026
News articlesThe TGA is updating information for nitrosamine impurities and other nitroso-structure impurities in medicines including acceptable intakes (AI).
Latest publications
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Scheduling decisions (final)This web publication constitutes a notice for the purposes of regulation 42ZCZS of the Therapeutic Goods Regulations 1990 (the Regulations).
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Scheduling submissionsFind out about the public submissions on scheduling matters referred to the ACMS
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Scheduling decisions (final)This web publication constitutes a notice for the purposes of regulation 42ZCZS and regulation of the 42ZCX Therapeutic Goods Regulations 1990 (the Regulations).