Expanding your food supplement business from United Arab Emirates to Australia requires comprehensive understanding of local regulatory requirements and compliance standards. Australia operates under the jurisdiction of Therapeutic Goods Administration (TGA), which sets stringent guidelines for product formulation, labelling, health claims, and safety documentation.
At Taylored Consultancy, we specialise in supporting United Arab Emirates-based food supplement companies navigating the Australia regulatory landscape. Our end-to-end compliance services ensure your products meet all necessary requirements for successful market entry, from formulation review and labelling compliance to Food Business Operator (FBO) registration and ongoing regulatory support.

We check your formula against UK and EU food regulations, making sure ingredients are permitted, within legal limits, and safe for consumers.
Depending on where you're selling, your food supplement may need official registration. We handle the paperwork so you don’t have to.
If you’ve got an audit or regulatory inspection coming up, we help you prepare, respond, and stay compliant without unnecessary stress.
Comprehensive assessment under Therapeutic Goods Act 1989 to determine if product is a Listed Medicine (AUST L) or Registered Medicine (AUST R) for ARTG entry requirements.
Full compliance review under Therapeutic Goods Advertising Code, ensuring permitted indications for listed medicines and all labelling meets TGA requirements for Australia.
Compilation of traditional use evidence or scientific substantiation, supporting documentation for claims, and all required technical data for TGA assessment and approval.
Health and nutrition claims are one of the biggest compliance risks in the industry. We make sure your claims are scientifically backed, legally sound, and won’t land you in trouble with regulators.
Complete Australian Register of Therapeutic Goods registration process, including formulation review, evidence compilation, and TGA submission for market approval in Australia.
TGA sponsor requirements assessment and application support, including manufacturing evidence, GMP compliance verification, and sponsor licensing for Australia market entry.
Post-market surveillance, adverse event reporting systems, continuous monitoring of TGA regulatory updates, and compliance maintenance for Australia market authorization.
If you're selling in the UK or EU, you need a registered Food Business Operator (FBO). We act as your UK or EU FBO, ensuring your business meets all legal requirements to trade safely.
Bethany has a wealth of experience in medical devices and is always providing a fantastic service. Having worked with Bethany on and off over the years I can safely say I would trust her regulatory advice. Thank you Taylored & the team!

We have been working with Bethany for 3 months now and are very impressed! She is super orgainsed, very knowledgable and does it all with a smile! Would highly recommend.
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Amazing! Went over and above working longer hours communicating with suppliers and getting all the relevant info. Quick to find solutions and overall very helpful. Thank you!
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