Homeopathic products of dilutions >1000 fold (4X) that do not contain human or animal material are exempt from ARTG and Good Manufacturing Processes (GMP) requirements. Homeopathic preparations greater than 4X (ie. all mother tinctures and 1X, 2X, and 3X homeopathic preparations) and those that contain human or animal material must be registered or listed on the ARTG (as above).
NHP Consulting can assess whether your homeopathic product requires registration or listing on the ARTG, and assemble evidence packages for health claim substantiation. We can prepare/submit applications for homeopathic products to the TGA, if necessary, as well as review promotional materials (labels, packaging, website, radio/TV advertisements) to ensure compliance with Australian regulations.
NHP Consulting will provide all regulatory documentation to achieve market compliance for the Australian marketplace.