Manufacturing for registered complementary medicines

You must comply with regulatory requirements when making, supplying, or distributing registered complementary medicines. 

Registered complementary medicines must be manufactured in accordance with legislated Good Manufacturing Practice (GMP) standards to ensure their quality, safety and efficacy. 

You are responsible for maintaining quality during production, supply, transport, and distribution.  

We regulate these activities to protect public health and ensure registered complementary medicines remain safe and effective. 

If you import or export registered complementary medicines, you must comply with Australian laws. 

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.