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Product

Everything the formulation record has to carry.

Capabilities below map to the product specification — formulation management, supplier-backed materials, market declarations, assessment, claims, and change impact.

Formulation management

Composition, yield, costing, and a clear version lifecycle.

Versions hold composition, declaration basis, yield factor, declared portion, target markets, and intended claims. Drafts stay editable; submissions become read-only; approvals freeze the decision and the data it relied on.

Formulation composition and findings workspace
  • Proportions to four decimal places, required to total exactly 100% before submission
  • Nested formulations that roll up allergens, nutrients, attributes, and cost
  • Batch scaling from finished quantity without mutating the version
  • States: Draft, In Review, Approved, Rejected, Superseded

Materials and suppliers

Supplier specifications as the unit of material identity.

Two suppliers of nominally the same material remain two specifications. Qualification gates use in approved formulations. New supplier versions do not silently rewrite what an approval already relied upon.

  • Legal names per language, never inferred
  • Intentionally present allergens distinct from cross-contact information
  • Nutrients including declared added sugars
  • Attributes that substantiate marketing claims
  • Cost in supply currency with organisation reporting currency roll-up

Market declarations & assessment

Derived label content and findings per territory.

Rule sets define allergen and nutrient vocabularies, rounding, declaration composition, QUID triggers, and claim conditions. Assessments produce advisory or blocking findings; incomplete data blocks approval without override.

Per-market declaration panels for UK, EU, and US
  • UK, EU, and US regimes with market-level national provisions
  • Declarations only when every required legal name exists
  • Traceability to supplier, nested formulation, and rule-set versions
  • Reassessment flags when supplier data or rules change

Bring market findings into the formulation desk.

Request early access if you are evaluating formulation software for UK, EU, and US product development.

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