Where Marco works
Every target market, one engine — each verdict cited to that country's own rule.
Listed-medicine ingredients, permissible-substance limits and the food-vs-therapeutic line — both sides of the boundary, cited.
Dietary supplements and the trans-Tasman food code, run through the same decidable engine.
Positive-list ingredients, dose ceilings and the RDC framework for supplements and foods.
NHPID monographs and NNHPD permitted routes — the licensed natural-health-product pathway.
Dietary-supplement admissibility, NDI status and the never-permitted lines under DSHEA. Decidable gates only — Marco never guesses a US 'permitted'.
Not seeing a market? We stand up new registers on request — the engine and the citations stay the same.
Keep regulatory review part of your product lifecycle.
Review current TGA ingredient requirements and the applicable FSANZ food standards for your exact formulation.
Ingredient limitsCheck the current ANVISA ingredient list, dose limits and product category, including amendments and corrections.
Category and doseVerify the current Health Canada monograph, licensing conditions and any recall or safety notice.
Licence and evidenceSee it on your products.
Start free — 4 checks, no card. Every verdict comes cited, or it comes honest.
Team plans & full details on the pricing page.