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EP1: An overview of Australian regulations

12 April 2021 Print

Join Sue Woldt, Senior Regulatory Affairs Manager at Integria Healthcare. Sue is a qualified naturopath, and over the last 30 years her experience spans across all areas of the Complementary Health Industry, specialising in Regulatory Affairs and Compliance.

In Part 1 of this 3 part series on Navigating the regulatory environment for complementary medicines, Sue provides a basic understanding of Australian regulations. 

Sue discusses:

  • Why complementary medicines are regulated in Australia, and how this differs from countries overseas
  • The Therapeutic Goods Association (TGA)- what they do and who they are
  • Why buy Australian Listed (AUST-L) products vs. those produced overseas
  • What is the difference between AUST-L vs. an AUST-R  medicines
  • What is a grandfathered product
  • Pre-approved ingredients and doses for use in AUST-L medicines

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