You must produce, handle and supply your registered complementary medicine in line with Australian regulatory requirements.
If you import or export registered complementary medicines, you must meet Australian regulatory requirements.
Understanding these requirements helps you meet legal obligations and manage risks throughout the supply chain.
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.
Supply
Understand your obligations to manage the ongoing supply of products.
Storage and handling
Access information about how the storage and handling of products is regulated.
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GuidanceGuidance for interpreting the Pharmaceutical Inspection Co-operation Scheme (PIC/S) guide to good manufacturing practice (GMP) for medicinal products.
Import and export
Access requirements for import and export of therapeutic goods.
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GuidanceThis guidance is to assist entities and individuals planning to export medicines (including prescription, over-the-counter (OTC) and complementary medicines) either for commercial supply, or for non-commercial purposes (for example, for a family member or friend).