Core
Multi-market declarations
Ingredient declarations, allergen expression, QUID where required, and nutrition values derived per UK, EU, and US rule sets and languages.
Design formulations with market findings in view.
Build recipes from supplier materials, then see cost, allergens, nutrition, claims, and UK–EU–US findings update as composition changes.
One authoritative formulation record. Findings while you design.
The problem
Recipes, labels, and claims should not live in different spreadsheets.
Ingredient declarations, allergen statements, nutrition panels, and claim eligibility are consequences of the recipe. Change an ingredient and all of them move — differently by market and by the language the label must use.
Hand-built workbooks silently miss 100% totals, leave nutrition stale after reformulation, hide allergens one level down in compound materials, and discover market conflicts after launch plans are already set.
Capabilities
Built for the work of formulation, not generic project tracking.
Capability
Claims with limits
Nutrition claims evaluated against structured conditions. Health claim wording presented for human assessment. Marketing claims mapped to supplier attributes.
Capability
Cost and batch scale
Roll up material cost into finished-product cost with yield. Scale a version to a trial or production batch without altering the recipe.
Core
Change impact
When a supplier specification, qualification, or rule set changes, affected drafts and approved versions are identified for reassessment.
How it works
From draft composition to market-ready approval.
Step 01
Compose
Add supplier materials or nested formulations at stated proportions. The product shows the running total, cost, allergens, nutrition, and claim status as you work.
Step 02
Assess markets
Target the territories you sell into. Findings explain where a version is blocked or advised against — and why — before you submit.
Step 03
Derive declarations
For each market and language, generate ingredient, allergen, and nutrition content from recorded legal names and rule-set data. Gaps are reported, never silently filled.
Step 04
Approve and retain
An authorised reviewer approves for specific markets and claims. The version becomes immutable and records the supplier data, nested versions, and rule sets relied upon.
What changes
One formulation record. Findings while you design.
- Composition stays market-neutral
- Author the recipe once. Declarations, claim outcomes, and findings are derived per target market and required language.
- Supplier specs stay authoritative
- Allergens, nutrients, attributes, legal names, usage limits, and cost come from versioned supplier material specifications — not from memory.
- Approval stays human
- The product calculates and reports. Qualified staff decide. Blocking findings from missing data cannot be waved away.
Professional responsibility
Informs qualified judgement. Does not certify legality.
Formulation Designer reports findings against the rule sets it holds. It does not generate precautionary “may contain” statements, does not machine-translate regulated terminology, and does not claim that a product is legal to sell. Approval for a market remains an act of an authorised person.