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If you're planning to bring a registered complementary medicine to market in Australia, this is your starting point.
You need to understand how we regulate these products and your obligations at each stage of your medicine’s lifecycle. This includes choosing the right pathway, preparing evidence and meeting all applicable quality and safety requirements.
Being well prepared helps ensure your product meets Australian requirements and avoids delays in getting your medicine approved.
Start by learning your responsibilities and planning each stage of your product’s lifecycle.
You must meet certain obligations to legally supply therapeutic goods in Australia. This section contains guidance and information specific to registered complementary medicines. You may also have to meet obligations that apply to all medicines and all products.