The First Multi-Market Food Supplement Compliance Software

Taama gives regulatory teams, brands, and consultants simultaneous AI-powered compliance verdicts across all your markets in minutes — covering every check type in a single product upload.

Book a Demo

See How it Works

Book a Demo

See How it Works

The First Multi-Market Food Supplement Compliance Software

Taama gives regulatory teams, brands, and consultants simultaneous AI-powered compliance verdicts across all your markets in minutes — covering every check type in a single product upload.

Book a Demo

See How it Works

Sequential Market Checks Are Killing Your Launch Timeline

Most teams check one market at a time — running BPOM after HSA, TGA after NPRA, each one a separate engagement with a separate consultant or spreadsheet. By the time all markets are reviewed, formulas are locked, artwork is briefed, and errors are expensive. Taama runs all target markets in parallel from one upload, returning a regulation-traced verdict across every market simultaneously — not sequentially.

Sequential Market Checks Are Killing Your Launch Timeline

Parallel Assessment Engine

All Markets Assessed at Once

One product upload triggers simultaneous compliance checks across every target market. A product entering five markets runs five full assessments in parallel — not one after another. Regulatory affairs teams get a complete multi-market picture before committing to formulation, artwork, or registration spend.

Complete picture before launch

Parallel not sequential checks

One upload, all markets checked

Classification First Scoping

Regulatory Classification Before Any Check Runs

Every product is classified into the correct regulatory category and go-to-market pathway per market before ingredient, label, or claims checks begin. Whether a product is AUST L or AUST R in Australia, Listed or Registered at HSA in Singapore, or MD versus ML under BPOM in Indonesia — classification drives the scope of every subsequent check.

No misclassification risk

Scopes all checks accurately

Know your GTM pathway per market

Regulation Traced Verdicts

Every Finding Linked to the Exact Regulation

Every verdict — across ingredient permissibility, label compliance, claims, and dossier completeness — is traced to the exact regulation, threshold, or policy that triggered it. Teams receive a pass-or-fix outcome they can act on and defend to a regulator, not a summary opinion or a database result to interpret manually.

Defensible audit-ready output

Pass or fix verdict per market

Exact regulation citation per finding

Speed And Scale

Assessments in Minutes Instead of Weeks

Compliance verdicts that previously required weeks of consultant engagement across multiple jurisdictions — TGA, FDA, HSA, BPOM, EFSA, Health Canada — are returned in minutes. Teams can screen new formulations early, run rapid iteration cycles without waiting for RA queues, and scale the number of markets without scaling headcount.

Minutes to multi-market verdict

Early-stage formulation screening

Scales without adding headcount

Common questions from regulatory and brand teams evaluating Taama's label compliance check capability.

Food Supplement Label Compliance Questions Answered

Taama covers 15 or more markets including Indonesia (BPOM), Malaysia (NPRA, MOH), Singapore (HSA, SFA, Nutri-Grade), Philippines (FDA PH), Australia (TGA, FSANZ), New Zealand (FSANZ, MPI), Gulf and GCC (SFDA, ESMA), EU (EFSA, EC 1924/2006, FIC), US (FDA, DSHEA, FTC), UK (FSA, MHRA), Canada (Health Canada, NHP), and Mexico (COFEPRIS, NOM-051). All markets are checked simultaneously from a single product upload.

Taama's assessment engine classifies a product into the correct regulatory category per market first — determining the applicable go-to-market pathway before any check runs. Once classified, ingredient permissibility, label compliance, marketing claims, and dossier completeness checks execute in parallel across all target markets simultaneously. Every finding is returned with the exact regulation, threshold, or policy that triggered it — not a generalized summary.

Taama returns compliance verdicts in minutes rather than weeks. The workflow runs from first upload through a product scan to targeted gap actions without sequential market-by-market delays. For teams currently managing multi-market compliance through consultants or internal RA queues, the reduction in review time is significant — enabling earlier formulation decisions and faster market access.

A single Taama assessment covers five compliance dimensions simultaneously: ingredient permissibility and dosage thresholds, regulatory classification and go-to-market pathway, label and packaging compliance, marketing and on-pack claims compliance, and registration dossier completeness. All five are assessed across all target markets in one upload — no separate modules or sequential workflows required. After launch, Taama also monitors the live portfolio and alerts teams when thresholds change, certificates expire, or claims are reclassified.

Taama uses a tailored pricing model. All plans are custom-scoped based on your target markets, product catalogue, and team size — you pay only for the coverage you need. There are no fixed tiers or published plan prices. Contact Taama directly to receive a scoped quote based on your specific market footprint and SKU volume.

Common questions from regulatory and brand teams evaluating Taama's label compliance check capability.

Whether you’re navigating TGA and FSANZ in ANZ, HSA in Singapore, BPOM in Indonesia, NPRA in Malaysia, EFSA in Europe, or FDA in the US, Taama runs the checks.

Launch faster with Taama

Talk to the Taama team and see how simultaneous multi-market compliance verdicts work on your actual products and target markets.

Book a Demo

Whether you’re navigating TGA and FSANZ in ANZ, HSA in Singapore, BPOM in Indonesia, NPRA in Malaysia, EFSA in Europe, or FDA in the US, Taama runs the checks.