Is there a free trial?

Yes — 7 days, 2 full assessments, no credit card required. Upload a real product and pick your target markets. You'll get a structured compliance assessment covering all five check types before you pay anything.

Image of a regulatory manager reviewing a packaging.

For Food and Supplement Brands

A Compliance Platform Built for CPG Complexity

Taama checks your products against the regulatory rules of multiple markets simultaneously - returning a regulation-traced pass-or-fix verdict in minutes, not weeks.

Catch restricted ingredients, label gaps, and claims issues before they delay your launch. Purpose-built for global markets — including APAC, EU, US, ANZ and more — where coverage depth and multi-market checks matter.

Book a Demo

See How It Works

Where Generic Compliance Tools Let CPG Brands Down

Months lost checking markets one at a time.
Individual market-by-market reviews stack delays across your NPD cycle, consuming team bandwidth before a single SKU even reaches the shelf.
Formula locked, ingredient blocked by FDA.
A restricted ingredient or exceeded threshold surfaces after formulation is locked, forcing costly reformulation and delaying your entire market entry timeline.
Label reprinted after compliance gap found.
Packaging artwork goes to print before label elements are validated, turning a compliance gap into a reprinting cost and a missed retailer window.

Stop guessing. Stop chasing documents. Stop hoping you got it right.

Upload one product and Taama simultaneously checks ingredient permissibility, regulatory classification, label compliance, claims, and dossier completeness across all your target markets at once. Every verdict is traced to the exact regulation or threshold so your team acts on evidence, not guesswork.

After launch, Taama monitors your live portfolio and alerts you before a change becomes a violation.

Food and supplement brands today, beauty and pet food next; across TGA and FSANZ in ANZ, HSA and SFA in Singapore, BPOM in Indonesia, NPRA and JAKIM in Malaysia, EFSA in the EU, and FDA in the US.

4 capabilities.
One outcome: a brand that scales confidently.

Each one removes a specific bottleneck so your team spends less time on process and more time on impact.

Ingredient screening before formula is locked

Taama screens every ingredient against permitted and restricted lists across your target markets simultaneously, flags threshold breaches, and returns exact regulation citations - so decisions are made on facts before the brief leaves R&D.

Image of a supplement registration dossier.

Regulatory classification before your GTM pathway is set

Food vs supplement, Listed vs Registered, MD vs ML. Taama determines the go-to-market pathway before any other check runs, ensuring every downstream verdict is scoped correctly for the product type in your target market.

Get a definitive verdict.

Food vs supplement, Listed vs Registered, MD vs ML, one clear classification and pass-or-fix answer per market, traced back to the regulation it's based on. Not a list of options, not an opinion you can't verify.

Labels cleared before artwork goes to print

Taama reviews on-pack declarations, allergen panels, NIP format, Nutri-Grade requirements, and all country-specific mandatory elements against each market's labeling rules - returning a clear pass-or-fix verdict with the exact gaps identified.

Pull every document into one place.

Track submissions, approvals, and requirements in one place.
See what’s in progress, what’s blocked, and what’s next. Your team can coordinate without delays or misalignment.

Claims reviewed before copy goes live

Taama evaluates every product claim against each market's permitted claims framework, so your brand never oversteps without knowing it.

Monitor it after launch.

A threshold changes, a certificate expires, a claim gets reclassified? Taama catches it across your live portfolio and tells you before it becomes a recall.

One system across every market, SKU, and partner.

From first validation to ongoing monitoring, everything is tracked in one place.
No blind spots. No fragmented workflows. Just clear visibility and execution as you scale.

From the field

Business team collaborating on laptops and documents around a table.

"Managing 60 supplement products across markets, Taama helps us stay ahead of regulatory changes across our markets and move fast when something shifts."

SINGAPORE BASED SUPPLEMENT BRAND

Problems rarely start big. Something missing, something unclear, something caught too late, that's where timelines slip and revenue goes with them. Taama replaces the guesswork with one AI system that checks, monitors, and surfaces issues early, before they cost you.

Markets covered across APAC, EU & Americas

Faster to launch

Product Assessment

FAQ

Frequently Asked Questions

Everything you need to know about how Taama works, which markets we cover, and how pricing works.

Ingredient permissibility, regulatory classification and GTM pathway, claims, label and packaging compliance, registration dossier completeness, and document validity, across all your target markets in one assessment.

18 markets including Australia (TGA, FSANZ), New Zealand, Singapore (HSA, SFA), Indonesia (BPOM, MUI), Malaysia (NPRA, JAKIM), Philippines, EU (EFSA), Gulf/GCC (SFDA, ESMA), US (FDA, DSHEA), UK (FSA, MHRA), Canada (Health Canada), and Mexico (COFEPRIS). China coming soon. Vietnam, Thailand, India, South Korea, and Japan on our roadmap. Yes. If your market isn't covered yet, just ask, we add markets on demand. Reach out and we'll let you know what's possible!

One product across one target market - all five check types included. A product targeting three markets uses three assessments. The Starter Plan includes 10 assessments per month.

Taama is built for three groups. Food and supplement brands use it to launch and manage products across multiple markets without a regulatory team in every country. Regulatory consultants and agencies use it to review products faster on behalf of clients and scale capacity without adding headcount. Retailers and supermarkets use it to assess supplier product risk before listing — checking ingredients, labels, and documentation in seconds rather than days.

Still have questions?We're here to help.

Contact Support →

See it on your products. 30 minutes.

Pick a time below and we'll walk through your markets, products, and compliance gaps live.

A Compliance Platform Built for CPG Complexity

Where Generic Compliance Tools Let CPG Brands Down

Months lost checking markets one at a time.

Formula locked, ingredient blocked by FDA.

Label reprinted after compliance gap found.

Stop guessing. Stop chasing documents. Stop hoping you got it right.

4 capabilities. One outcome: a brand that scales confidently.

Ingredient screening before formula is locked

Ingredient screening before formula is locked

Regulatory classification before your GTM pathway is set

Get a definitive verdict.

Labels cleared before artwork goes to print

Pull every document into one place.

Claims reviewed before copy goes live

Monitor it after launch.

One system across every market, SKU, and partner.

Frequently Asked Questions

See it on your products. 30 minutes.

4 capabilities.
One outcome: a brand that scales confidently.