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
Stay informed as a health professional on safety issues and changes to product information for medicines and medical devices. -
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
Read about safety problems reported for medicines and medical devices, and any actions you need to take. -
Medicine shortage alerts
Find information about medicine shortages, how long we expect them to last and available alternatives. -
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. -
Report a medical device incident - 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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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 our decision trees to work out classifications, advertising and manufacturing questions, and product types. -
Resources
Search our resources for checklists, user guides, international scientific guidelines, compositional guidelines and forms.
Latest articles
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TGA releases updated social media advertising guidance to support improved compliance
Media releasesThe TGA has updated its Advertising therapeutic goods on social media guidance to help advertisers to understand their responsibilities when promoting therapeutic goods via these platforms. -
ACPharm Queensland issued infringement notices for alleged unlawful advertising of therapeutic goods
Media releasesWe have issued 5 infringement notices, totalling $99,000, to ACPharm Queensland Pty Ltd (ACPharm Queensland) for the alleged unlawful advertising of therapeutic goods. -
Nitrosamine impurities acceptable intakes update - November 2025
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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Meeting statementsFind out about the AIVC Recommendations for the Composition of Influenza Vaccines for Australia in 2026.
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TGA laboratory testing reportsThe Therapeutic Goods Administration (TGA) is issuing a safety advisory regarding imported unregistered melatonin products following testing by TGA Laboratories.
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Scheduling decisions (final)Publication of the decisions made by a delegate of the Secretary