Business Capability Directory

Turn scattered supplier quotes and email threads into defensible, weighted scorecards in minutes.

Eliminate manual retyping of recipe, nutrition, and allergen data into retail B2B customer portals without transcription errors.

Turn raw auditor notes and non-conformities into an audit-ready IFS corrective action plan within the 14-day submission window.

Find a co-packer in 2 minutes instead of 2 weeks, filtered by region, certification, MOQ and category.

Know before you spend sourcing and labelling budget whether an ingredient is an unauthorised novel food.

Find the banned or restricted ingredient while the formulation can still be changed, not during the safety assessment.

Identify undeclared priority allergens, missing sub-ingredients, and improper allergen formatting before packaging artwork is printed.

Catch nutritional tolerance deviations and undeclared allergens at the dock before raw materials are released into manufacturing.

Audit published private-label product nutrition sheets against GS1 GDSN master specifications and prevent e-commerce mismatches, GDSN validation errors, and allergen barcode rollover failures.

Detect unannounced supplier reformulations, ingredient substitutions, and cheapflation before affected batches enter production.

Disaggregate competitor recipes mathematically from shelf packaging data and identify clean additive alternatives before R&D formulation.

Catch the allergen that needs bold type on the ingredients list before the label goes to print, not after a recall.

Know whether GM presence in food or feed triggers mandatory labelling or 5-year traceability record transmission before packaging sign-off.

Know which constituents need a weight-percentage band or an allergen listing on pack, before the artwork is signed off.

Know specific migration limits, PFAS concentration thresholds and BPA ban rules before finalizing food packaging artwork or material specifications.

Know what an E-number is actually approved for before it goes on your ingredient list, not after a retailer flags it.

Audit vitamin and mineral formulations, mandatory units, and E171 additive prohibitions before packaging artwork sign-off.

Know permitted chemical sources, prohibited food categories, and Annex III restriction limits before launching fortified foods.

Catch an unauthorised health claim before artwork goes to print, with the register entry cited.

Evaluate food additive authorizations, thermal stability thresholds, and MIXTOX cumulative hazard index for recipe formulations against official EFSA OpenFoodTox 3.0 benchmark data.

Assess supplier chemical safety risk scores based on EFSA OpenFoodTox toxicological profiles and RASFF notification history.

Evaluate pesticide MRL exceedances and PRIMo acute/chronic dietary exposure against EFSA OpenFoodTox 3.0 benchmark data.

Verify raw material specification limits and heavy metal purity criteria against EFSA OpenFoodTox 3.0 and EU contaminant rules.

Audit toxicological study quality and Weight of Evidence for ingredient safety dossiers according to official EFSA and SCHEER criteria.

Evaluate chemical contamination incidents and lab COAs against EFSA OpenFoodTox toxicological limits and prevent unnecessary public recalls.

Know exact EU pesticide residue limits and measurement uncertainty deductions before importing or releasing batches.

Turn a recipe into a print-ready nutrition panel in seconds, correctly rounded to the FIC rules, instead of building one by hand in a spreadsheet.

Prevent ETL pipeline blackouts and faulty statistical calculations in automated Eurostat data ingestion workflows.

Prevent pricing errors and contract adjustment disputes by validating Eurostat food price index queries, ECOICOP v2 mappings, and 2025=100 rebasing calculations.

Prevent retroactive (ex tunc) clause voidness and avoid supplier refunds by validating price adjustment clauses before execution.

Calculate weighted price adjustments and updated unit target prices with transparent Eurostat index breakdown for B2B negotiations.

Benchmark B2B supplier price increases against official regional industry price indices and build objective supplier development scorecards.

Know the exact date-marking wording and precision a product needs before packaging goes to print, not after a recall.

Find out that a raw material or supplier has already been recalled somewhere while it can still be kept out of the specification, instead of learning it from a pathogen result.

Know which bottle sizes and container volumes are legally permitted before packaging artwork and molds are finalized.

Know whether a recipe passes the 95% organic threshold and what logo co-location rules apply before artwork sign-off.

Find out before artwork whether saying "Made in Italy" obliges you to also say where the main ingredient came from, and in which exact wording.

Get defensible USDA nutrition database composition numbers and compare US nutrition facts database declarations in minutes without manual lab lookups. FDA rounding and Daily Values stay a separate regulatory step.

Turn a recipe into a compliant nutrition table, including reference intakes and rounding rules.

Skip formulation entirely where a supplier already has a product you can brand.

Catch a broken barcode before it reaches a retailer listing sheet.

Evaluate incoming raw material shipments for chemical hazards at the warehouse gate and resolve trace contaminant alerts in seconds.

Screen food contact material migration values against EU SML limits, Regulation (EU) 2024/3190 BPA prohibitions, and EFSA OpenFoodTox benchmarks.

Evaluate food additive authorizations, thermal stability thresholds, and MIXTOX cumulative hazard index for recipe formulations against official EFSA OpenFoodTox 3.0 benchmark data.

Format required Critical Tracking Event (CTE) and Key Data Element (KDE) records for FDA 24-hour FSMA 204 inspection requests and identify missing lot codes before audits.

Structure foreign supplier verification records for FDA inspections and identify expired annual audits or missing hazard evaluations before PCQI review.

Turn raw GFSI audit non-conformities into 5-Whys root cause prompts and structured CAPA plans within required submission windows.