Manage Your Product Documents & Dossiers In One Place

Taama's AI platform checks registration dossier completeness across 12 live markets simultaneously, identifying missing certificates and document gaps before submission to prevent costly rejections.

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See How it Works

Book a Demo

See How it Works

Manage Your Product Documents & Dossiers In One Place

Taama's AI platform checks registration dossier completeness across 12 live markets simultaneously, identifying missing certificates and document gaps before submission to prevent costly rejections.

Book a Demo

See How it Works

Dossier Gaps Discovered After Submission Cost You Markets

Regulatory teams building dossiers for BPOM, HSA, TGA, FDA, or EFSA face the same failure mode: a missing certificate or incomplete specification surfaces only after submission, triggering rejection and restarting the clock. Spreadsheets and shared drives cannot track completeness per market, flag expiring certificates, or control what partners see. Taama's dossier engine runs completeness checks before you submit, linked to the exact regulation that requires each document, across every target market at once.

Dossier Gaps Discovered After Submission Cost You Markets

Pre-Submission Validation

Catch Document Gaps Before Regulators Do

Before any dossier reaches a regulator, Taama identifies every missing specification, certificate, or required document per target market. Each gap is linked to the exact regulation that mandates it, giving your team a targeted fix list rather than a rejection letter.

Covers specs, CoA, GMP and more

Exact regulation cited per gap

Market-specific completeness assessment

Expiry and Renewal Alerts

Proactive Alerts Before Certificates Expire

Taama tracks every certificate and compliance document in your dossier portfolio and issues proactive alerts before expiry dates are breached. Regulatory affairs teams managing registrations across markets like Australia, Singapore, the Philippines, and the GCC no longer need manual calendar tracking to avoid lapses.

Covers all markets in your portfolio

Alerts before deadlines are missed

Automated expiry date monitoring

Secure Partner Access

Share Dossier Sections Without Exposing Everything

When distributors or external partners need dossier documents, controlled sharing lets you expose only the specific sections required, not the full dossier. This protects proprietary formulation data while giving partners and in-market agents exactly what their local regulator requires for submission.

Audit-ready access management

Distributor access without full exposure

Granular sharing controls per section

Single Source of Truth

Centralize All Product Compliance Documents

Taama consolidates every product's compliance documentation across all target markets into a single structured workspace. Submission status, document versions, and certificate validity are tracked per SKU per market, eliminating the version control failures and scattered files that delay registration decisions.

All SKUs and markets in one place

Specs, CoA and certificates organized

Submission status tracked per market

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

Food Supplement Label Compliance Questions Answered

Taama covers 12 live markets including Indonesia (BPOM), Malaysia (NPRA, MOH), Singapore (HSA, SFA), Philippines (FDA PH), Australia (TGA, FSANZ), New Zealand (MPI, FSANZ), the GCC (SFDA, ESMA), the EU (EFSA, EC 1924/2006, FIC), the US (FDA, DSHEA), the UK (FSA, MHRA), Canada (Health Canada), and Mexico (COFEPRIS, NOM-051). Dossier completeness requirements, certificate mandates, and submission structures are maintained per market and updated continuously.

Taama's assessment engine first classifies your product into the correct regulatory category for each target market — for example, AUST L, Listed or Registered under HSA, or MD versus ML under BPOM. Once classification is set, the engine maps the exact document requirements that apply to that product type in that market and compares them against what has been uploaded. Every identified gap is returned with a citation to the specific regulation or guideline that mandates the missing document.

Taama runs all market assessments in parallel, not sequentially. A product targeting five markets returns five completeness assessments simultaneously. The overall review takes minutes rather than the days or weeks typically required when building and validating dossiers manually or market by market. This speed advantage compounds when managing a large SKU portfolio approaching regulatory submission deadlines.

Yes. Taama supports controlled dossier sharing at the section level. You select which documents or sections a distributor, in-market agent, or external partner can access. The remaining dossier, including proprietary formulation specifications or commercial data, is not visible to that party. This allows compliant information exchange with partners across markets without creating data exposure risks or requiring manual file redaction.

Taama does not publish fixed plan tiers. All plans are custom-scoped based on your target markets, product catalogue size, and team structure. This means you only pay for the market coverage and document volume relevant to your portfolio. Contact Taama directly to receive a scoped quote aligned to your registration programme.

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.

Book a Dossier Review Demo

See how Taama checks registration dossier completeness across your target markets and identifies document gaps before submission. Book a demo with the team.

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.