We take your idea to a finished, listable formula: ingredients, dose, format and claims, designed to Australian rules from the first draft.
Who it is for, what it should do and where it will sell.
Ingredients, dose and the evidence behind each one.
Every ingredient checked against the permitted list.
Capsule, tablet, powder or gummy, matched to the formula.
Each claim linked to a permitted indication.
Samples, stability and the tests the listing needs.
Founders, growing brands and anyone adding a product.
Product development runs on Plumb Line, the people. Every decision is tracked in Get Plumb, and once you launch, Stay Plumb keeps watching the claims.
Choosing and managing a GMP licensed manufacturer and suppliers, from pilot batch to scale.
Learn more →04Stability, potency and micro testing, planned and read for you.
Learn more →02AUST L listings, sponsor obligations and evidence packages, prepared and kept current.
Learn more →It depends on the formula, the format and the maker. Your roadmap sets a timeline before work starts.
Yes. We work with your maker, or help you choose one that is GMP licensed for your format.
Yes. Every claim is mapped to permitted indications while the formula is designed, not after.

Tell us where your product is at, and we will come back with a plan.