For over 20 years we have been providing expert regulatory and technical advice for companies with products going into markets in Australia, New Zealand and USA.

We provide regulatory advice for

  • Complementary medicines ( or 'dietary supplements')
  • Foods
  • Cosmetics, personal hygiene and domestic cleaning products
  • Medical devices

Our in-house technical team all have university qualifications in relevant disciplines including science, botanic medicine, human nutrition and marketing.

Our team of specialists will:

  • Review your existing formulations for compliance
  • Search for suitable information to support your product's claims
  • Determine what you can say on your promotional material, including websites, labelling and packaging, and in media advertising
  • Prepare applications to Government agencies including health and quarantine departments

With our strong international links, we can also help companies wishing to export from Australia to key markets around the world.

Receive regulatory news as it happens! This is published on our website, and is also available through Twitter, or by subscribing to our popular e-newsletter.

How do we provide our advice    |    News Centre

Our in-house technical team all have university qualifications in relevant disciplines including science, botanic medicine, human nutrition and marketing. 

Our team of specialists will:

RFA Breaking News

TGA Latest Fee & Charge Summary as of 1 July 2016

The TGA is required to recover its costs for all activities that fall within the scope of the Therapeutic Goods Act 1989, including the TGA's public health responsibilities. A fee…

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TGA Webinar on International Harmonisation of Ingredient Names

On 10th June 2016, Jola Samoc of the Therapeutic Goods Administration, delivered an online webinar on the topic of ‘Updating Medicine Ingredient Names’. This PDF summary outlines in a very…

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TGA Annual Charge Exemption Scheme: Q & A

On 10th June 2016, Jola Samoc of the Therapeutic Goods Administration, delivered an online webinar on the topic of ‘Updating Medicine Ingredient Names’. This PDF summary outlines in a very…

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TGA Puts Spotlight on Listed Medicines With Blood Glucose And Cholesterol Indications

The TGA will be initiating targeted compliance reviews for Listed medicines that have indications relating to blood glucose or cholesterol biomarkers. They will be focusing on medicines that have a…

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TGA Progress Stalls on MRA GMP Clearance Application Processing Times

As of 7 June 2016, the average processing time taken to complete an MRA GMP clearance application was 6.6 weeks. 90% of the finalised MRA GMP Clearance applications were within…

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TGA Safety Advisories for July:

Black Storm tablets  The Therapeutic Goods Administration (TGA) has tested product labelled Black Storm tablets and found that the tablets contain the undeclared substances sildenafil and vardenafil (actives in Viagra…

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