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
If you're travelling to or from Australia, bring 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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Datasets
Search the Australian Register of Therapeutic Goods (ARTG), and safety alerts, product shortages, approvals, and regulatory actions. -
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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Listed Medicine Compliance Reports - March 2026 Update
News articlesWe’ve updated the Listed Medicine Compliance Reports database with the results of compliance reviews covering 32 listed medicines. -
Improving the regulation of sunscreens in Australia
Media releasesWe have opened an 8-week public consultation seeking improvements to the regulation of sunscreens in Australia. -
TGA issues infringement notices to 3 health practitioners for alleged unlawful importation of therapeutic goods
Media releasesWe have issued 6 infringement notices totalling $23,760 to 3 health practitioners for the alleged unlawful importation of unapproved therapeutic goods.
Latest publications
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Meeting statementsAdvisory Committee on Medicines meeting statement
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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 of the Therapeutic Goods Regulations 1990 (the Regulations).