Australian regulators do not distinguish between medicines and complementary medicines when it comes to safety, efficacy and quality of the product, including the imported products!

Read the first part of this series – Regulatory Approval for Complementary Medicines in Australia Part-I – to understand what complementary medicines are and how they are classified in Australia.

To register herbal, animal, cosmetics, vitamins or minerals products in Australia, one needs to take the route of complementary registration process.

If you are interested in filing an application of your complementary medicine in Australia, let’s understand how TGA ensures the safety, quality and efficacy of complementary medicine.

TGA approval process for complementary medicine

Whole process needs to be considered in these six parts before making product application to TGA.

  1. Active ingredient
  2. Therapeutic claim
  3. Quality of the finished product
  4. Safety data
  5. Label and Advertisement of the product
  6. Australian based Sponsor

Let’s understand them one by one.

1. Active ingredient

Sponsor needs to ascertain first, whether their active ingredients (active and non-active) are listed on the TGA website for permissible active ingredient list.

The 26BB Legislative Instrument provides a list (26BB list) of all ingredients available for use in listed medicines.

If active ingredient is registered on 26BB list, it is fairly easy for manufacturer to proceed with the listing or registration of such products, provided he complies with other TGA requirements for registration of such products.

If the active ingredient is not available on this list, it is treated as New Substance by TGA and applicant has to start the process from registration of active ingredient. Comprehensive dossier needs to be prepared and submitted to TGA for evaluation of active ingredient.

Classification of ingredient evaluation

There are four different categories for the evaluation of active ingredient by TGA.

 

Legend: (COR = comparable overseas regulator)

Based on the safety and quality data available along with regulatory filing status in other regions, sponsors can decide upon the category under which they would like to file application to TGA.

Remember! Evaluation time frame, application requirements and fees vary for each category!

Discuss your product details with us to ascertain the category for your product’s successful registration in Australia.

Provide brief info on your product and registration requirements.
Provide your work email, where we can contact you

2. Therapeutic Claim

  • TGA Website provides a list of the permissible indications for use for listed complementary medicines.
  • It is a legal requirement that the sponsor of the product hold acceptable evidence to support the product’s therapeutic claim.
  • Evidence can be based on traditional use or scientific evidence.
  • Sponsor has to prepare a bibliography/summary table of the evidence and references that support your product’s indications for use while applying to TGA.
  • If your product is chosen by TGA for full evaluation (TGA does not fully evaluate all products, but select some), for the post marketing product assessment, the sponsor has to provide a bibliography/summary table of the evidence you have used to support the therapeutic claim/ indications.

3. Quality of the finished product

Two main points needs to be considered when it comes to managing the quality of the finished product.

  1. How is it manufactured (GMP aspect)?
  2. What are quality control measures in place?

TGA does not specify any GMP requirements for active ingredients. It’s only for finished products.

GMP aspect

  • The Australian Code of GMP is entirely based on the international standard Guide to Good Manufacturing Practices for Medicinal Products, published by the Pharmaceutical Inspection Cooperation Scheme (PIC/S).
  • Each Australian manufacturer of medicinal products for human use to hold a manufacturing licence.
  • General information for manufacturers are provided on TGA website for Australian manufacturing licenses and overseas GMP certification.
  • All complementary medicine supplied in Australia must be manufactured in a facility that has been inspected for compliance with medicinal GMP.
  • Australia has a Mutual Recognition Agreement (MRA) with some countries. However if your products are not manufactured in one of these countries, then the TGA may need to visit the factory and perform an inspection for GMP compliance, unless they have been inspected by a regulator recognised by the TGA, in which case an off-site documentation audit would be undertaken.

Quality control measures

The Act defines the quality standards applicable to all therapeutic goods.

  • To ensure the quality of the product, the sponsor must ensure that they adhere to default standards recognised in the Therapeutic Goods Act 1989, that is, the British Pharmacopoeia, United States Pharmacopoeia – National Formulary and the European Pharmacopoeia.
  • If the ingredient is subject to a default standard, you have to comply with applicable standard.
  • The TGA considers the suitability of other national or international pharmacopoeial monographs or standards for a substance on a case-by-case basis.
  • In many instances, there are no applicable monographs, in such cases compositional guidelines must be developed by the sponsor.
  • A compositional guideline is a summary of descriptions, tests and limits that defines the composition and relevant characteristics of the substance, where the pharmacopoeial monograph or standard sufficiently characterises the substance, is not available.

4. Safety Data

Complementary medicine in Australia, is classified based on the risk associated with the ingredient.

The sponsor must provide sufficient information on

  • Literature search data,
  • Toxicological data,
  • Biological activity data,
  • Clinical trial data and
  • Adverse reaction

to prove the safety and efficacy of the product

If product is derived from animal source or human source, sponsor may have to support the dossier with additional safety data.

Do you know that QUALITY & SAFETY are the two most important considerations for TGA? Ascertain that your filing matches the criteria.

Way forward to effective dossier preparation

It’s imperative for sponsors to make comprehensive dossier for their product and submit to TGA.

With all supportive evidences, particularly those related to quality and safety, your dossier stands strong for a thorough evaluation by TGA.

But,

There are two other important aspects of dossier – Label & advertisement sponsor – that need to be considered to make dossier complete in all aspects.

It’s a long wait for approval after dossier submission to TGA based on the category you have chosen for your product. The last thing you want from TGA after this waiting period is query (or, queries), which can cost you costly delays in product launch.

So be cautious.

We will be covering up remaining important aspects and salient features for a flawless submission process, along with post marketing review and adverse event reporting aspects in the last and concluding part of this series.

Stay tuned for part III in this series.

Talk to us now, for making your Complementary Medicine application to TGA a success?

Provide preliminary details below and we will help you achieve a successful registration in Australia.

Provide brief info on your product and registration requirements.
Provide your work email, where we can contact you

Reference:

1. https://www.tga.gov.au/complementary-medicines
2. https://www.tga.gov.au/overview-regulation-complementary-medicines-australia
3. https://www.tga.gov.au/standards-guidelines-publications-complementary-medicine
4. https://www.tga.gov.au/publication/australian-manufacturing-licences-and-overseas-gmp-certification