Where Marco works

Every target market, one engine — each verdict cited to that country's own rule.

AULive
Australia
TGA · FSANZ

Listed-medicine ingredients, permissible-substance limits and the food-vs-therapeutic line — both sides of the boundary, cited.

NZLive
New Zealand
FSANZ · MPI

Dietary supplements and the trans-Tasman food code, run through the same decidable engine.

BRLive
Brazil
ANVISA

Positive-list ingredients, dose ceilings and the RDC framework for supplements and foods.

CALive
Canada
Health Canada

NHPID monographs and NNHPD permitted routes — the licensed natural-health-product pathway.

USLive
United States
FDA · DSHEA

Dietary-supplement admissibility, NDI status and the never-permitted lines under DSHEA. Decidable gates only — Marco never guesses a US 'permitted'.

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On demand

Not seeing a market? We stand up new registers on request — the engine and the citations stay the same.

Regulatory intelligence, live

And after launch — the changes we caught, so you don't reformulate blind.

AUFeb 2026

TGA reissued the Permissible Ingredients Determination — dose limits re-ingested across 5,000+ ingredients.

Ingredient limits
BRJun 2025

A DOU retificação quietly moved ANVISA's creatine cap from 3 g to 5 g per day, eight days after IN 373/2025.

Dose cap correction
CAApr 2026

Health Canada updated NHP monograph dose caps — folded into every Canadian verdict.

Monograph update

See 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.