Run Your Ingredient Permissibility Check Across Every Market at Once

Taama runs a food supplement ingredient permissibility check across 15+ markets simultaneously, returning regulation-traced pass-or-fix verdicts for every ingredient in your formula in minutes.

Book a Demo

See How it Works

Book a Demo

See How it Works

Run Your Ingredient Permissibility Check Across Every Market at Once

Taama runs a food supplement ingredient permissibility check across 15+ markets simultaneously, returning regulation-traced pass-or-fix verdicts for every ingredient in your formula in minutes.

Book a Demo

See How it Works

Most Ingredient Failures Surface After the Formula Is Locked

When a restricted or threshold-exceeded ingredient is discovered late in development, the entire project resets — reformulation, restaging, missed retailer windows. Checking markets one at a time against fragmented regulatory sources like BPOM, HSA, TGA, NPRA, FDA, and EFSA is slow, error-prone, and never fully current. Taama screens every ingredient in your formula against permitted substance lists, dosage thresholds, and market-specific prohibitions across all target markets simultaneously, returning a GO, FIX, or REVIEW verdict per ingredient per market with the exact regulation citation.

Most Ingredient Failures Surface After the Formula Is Locked

Dosage and Use-Level Compliance

All Target Markets Checked in One Upload

One formula upload triggers ingredient permissibility checks across every target market in parallel. Indonesia BPOM, Malaysia NPRA, Singapore HSA, Australia TGA and FSANZ, Philippines FDA, EU EFSA, US FDA and DSHEA, and 10+ additional markets are assessed at the same time, not sequentially. No switching between databases or running separate checks per market.

Single upload replaces multi-tool workflow

GO, FIX, or REVIEW verdict per ingredient per market

15+ global markets checked in parallel

Multi-market ingredient permissibility check

Ingredient Dosage Permissibility Threshold

Ingredient Permissibility and Authorization Checks

Threshold Breaches Flagged With Exact Citations

Permissibility is not binary. Many ingredients are permitted up to a specific dosage, use level, or target population, and the thresholds differ by market. Taama checks the declared use level of every ingredient against the exact limit set by each regulator, flagging any breach with the precise regulation reference — not a general warning.

Population-specific restrictions surfaced early

Exact regulatory citation for every flag

Use-level checked against per-market thresholds

Custom and Restricted Substance Lists

Novel Food Status Identified Before Submission

An ingredient with a safety profile in the US or EU may have no novel food authorization in Singapore, Australia, or the Philippines, blocking market entry entirely. Taama identifies novel food authorization gaps per market so your team knows which ingredients require additional regulatory pathway work before the formula is finalized.

Pathway requirements flagged per jurisdiction

Authorization gaps identified before formula lock

Novel food status checked per market

custom-substance-list-screening

Screen Against Custom Lists Including WADA

Beyond regulatory permitted lists, some categories require screening against additional reference lists. Sports and performance nutrition brands can run ingredient checks against anti-doping and WADA substance lists. Retailer-specific approved ingredient lists and brand-defined exclusion lists are also supported, so every check reflects your actual go-to-market constraints.

WADA and anti-doping substance screening

Brand-defined exclusion lists supported

Retailer-specific approved list checks

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

Food Supplement Label Compliance Questions Answered

The check covers 15+ markets including Indonesia (BPOM), Malaysia (NPRA and MOH), Singapore (HSA and SFA), Philippines (FDA PH), Australia (TGA and FSANZ), New Zealand (FSANZ and MPI), Gulf and GCC markets, the EU (EFSA and EC 1924/2006 framework), the US (FDA, DSHEA, NDI requirements), the UK (FSA and MHRA), Canada (Health Canada NHP), and Mexico (COFEPRIS). Every verdict is traced to the specific regulation, threshold, or prohibited substance list that governs the ingredient in that market.

You upload a product — either from raw-material specifications or from the declared label ingredient list. Taama's assessment engine first classifies the product into the correct regulatory category for each target market, then screens every ingredient against that market's permitted substance lists, dosage thresholds, population-specific restrictions, and prohibited ingredient registers. The engine runs all target markets in parallel and returns a GO, FIX, or REVIEW verdict per ingredient per market, each linked to the exact regulation or threshold that generated the verdict.

From product upload, the multi-market ingredient permissibility check returns actionable verdicts in minutes. All target markets are assessed simultaneously rather than sequentially, which is what makes the turnaround possible regardless of how many markets you are targeting. The 2-minute setup and 3-minute scan workflow means a team can go from formula upload to a regulation-backed ingredient verdict across all target markets inside a single working session.

Yes. Taama does not reduce permissibility to a simple permitted or banned flag. For every ingredient, the check evaluates whether it is outright prohibited, permitted only up to a specific use level or dosage threshold, restricted to a particular product category or target population, or subject to additional authorization requirements such as novel food status. Where a threshold breach drives the verdict, the exact regulatory limit and the declared use level are both surfaced so your team knows precisely what needs to change.

All Taama plans are custom-scoped based on your target markets, product catalogue size, and team requirements. There are no fixed tiers or per-check fees listed publicly. Contact Taama directly to receive a scoped quote based on your specific market set and 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.

Screen Your Formula Across Every Target Market

Book a demo to see a live ingredient permissibility check run across your target markets with regulation-traced verdicts returned in minutes.

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.