Get plumb.
Stay plumb.
Compliance consultants for Australian brands.
What we do
We take products from idea to shelf, and keep them there.
Formula, manufacturer, testing, ARTG listing, label and claims. One team holds every step to the same standard, so nothing is fixed twice.
See every serviceWhy brands come to us
Most launches don’t fail on the formula.
They fail in the gaps between the formulator and the maker, the regulatory adviser and the agency.
A label is reprinted. A claim draws a TGA letter. A launch date slips while four advisers each fix their own piece. Plumb closes those gaps: one team owns the product from the first draft to the last claim.
Either it’s plumb, or it isn’t
Every formula, listing, label and claim we touch is held to the rules that apply today, and the ones on their way.
How a Plumb project runs
The work, the plan and the watch.
Every engagement has the same three parts. You deal with one team, see one plan, and stay covered after launch.
Plumb Line
Our consultants do the work, from the first formula to the final label.
Get Plumb
Our project platform. Every step, document and decision on one tracked plan you can see.
Stay Plumb
Our monitoring. Once you are on shelf, we keep checking your claims and the rule changes.
Start small
Begin with one piece of work.
A defined review with a clear outcome, so you can see how we work before committing to more.
Launch readiness review
For a new productConcept, ingredients, claims, label and manufacturing checked before you commit.
Ask about thisTGO 116 label review
For the 2031 deadlineEvery label in your range mapped to the new standard, with a transition plan.
Ask about thisRange compliance sweep
For products on shelfYour range across pack, web and social, with the fixes ranked.
Ask about thisWhat happens when you enquire
From first call to a written plan.
Plain answers, with sources.
What does a supplement regulatory consultant do?
A supplement regulatory consultant helps a brand develop, list and market a product that meets Australian rules: formulation within permitted ingredients, ARTG listing, labels, and claims that stay within permitted indications and the Advertising Code.
How do I list a supplement on the ARTG?
Most supplements are listed medicines, shown by an AUST L number. The Australian sponsor certifies the product uses permitted ingredients, makes only permitted indications, is made by a GMP licensed manufacturer and is backed by evidence held on file, then lodges the listing with the TGA.
Do I need an Australian sponsor?
Yes. Every product on the ARTG needs a sponsor based in Australia, and the sponsor is legally responsible for it.
What is TGO 116?
The TGA label standard for non prescription medicines. It commenced on 30 September 2026, and existing labels have until 1 October 2031 to comply.
Can you help with a TGA warning letter?
Yes. We review what the letter covers, fix the claims or labels involved and plan your response.
Do you work with start ups?
Yes. No project is too big or too small, from one label to a full range.
No project too big or too small.
Tell us where your product is at, and we will come back with a plan.