Document Intelligence for Food & Beverage

Food and beverage companies juggle formulations, ingredient specs, CoAs, and label requirements across hundreds of products , and label errors alone caused $1.92 billion in recall costs last year. Customiser's AI agents verify certificates of analysis against your specifications, cross-reference allergen data across your supply chain, and check label compliance against formulation records, catching the documentation gaps that turn into recalls, batch holds, and audit findings.

How teams use Customiser

Verify CoAs, extract formulations, check label compliance, and automate allergen tracking across your supply chain.

Formulation / Recipe Extraction

Extract ingredient lists, percentages, processing instructions, and allergen declarations from formulation documents and recipe cards. Customiser handles varied formats , from R&D lab notebooks to legacy production recipes , and delivers clean structured data for your PLM or formulation management system.

Ingredient Spec Verification

Verify incoming ingredient specifications against your approved standards , checking parameters like moisture content, particle size, microbiological limits, and allergen status. Customiser compares supplier spec sheets against your requirements and flags any deviations before the ingredient enters production.

CoA Cross-Referencing

Cross-reference certificates of analysis from ingredient suppliers against purchase order specifications and your internal quality standards. Customiser checks every analytical result , potency, purity, contaminants, microbiological counts , against acceptance criteria, flagging out-of-spec values.

Label Compliance Checking

Verify product labels against formulation data and regulatory requirements. Customiser checks ingredient order, allergen declarations, nutritional values, and mandatory statements against the actual formulation and applicable regulations, catching compliance issues before products go to market.

Formulation Change Impact Analysis

When a product formulation changes , new ingredient, supplier substitution, adjusted percentages , Customiser cross-references every ingredient against your specification Knowledge Base, flags new allergen introductions, identifies label elements that need updating, and generates a structured change impact report. What typically takes a cross-functional team days becomes an automated workflow.

Supplier Audit Documentation Pre-Screening

Batch-process an entire supplier's document history , CoAs, corrective action responses, specification change notices, food safety certifications , to extract key quality metrics and generate a structured pre-audit summary. Customiser highlights reject rate trends, non-conformance patterns, and certificate expiry dates so auditors arrive with focused, data-driven audit plans.

Food & Beverage FAQ

Customiser's AI extraction agents parse CoA documents in any format , PDF, scanned images, spreadsheets , extract every test parameter including microbial counts, allergen declarations, chemical composition, and nutritional values, and automatically cross-reference results against your predefined ingredient specifications. Non-conformances are flagged instantly, eliminating hours of manual review that delay batch release decisions.
Yes. Customiser's multi-agent pipeline parses ingredient lists, allergen declarations, and precautionary allergen labeling from supplier spec sheets, product labels, and CoAs , even from scanned documents. It identifies all major allergens, cross-references them against your product formulation records, and flags any undeclared or newly introduced allergens. With undeclared allergens causing 34% of all US food recalls, automated allergen verification is a critical safety control.
Labeling errors are the single largest cause of food recalls, with 76.8% of major allergen recalls traced to inadequate label controls. Customiser cross-references label artwork data against master formulation records, ingredient specifications, and regulatory requirements in real time , catching a missing allergen callout, an outdated ingredient list, or a wrong nutritional panel before the label reaches the printer.
FSMA Section 204 requires companies to maintain Key Data Elements at Critical Tracking Events throughout the supply chain. Customiser ingests supplier documentation in any format, extracts the required KDEs using custom extraction schemas, and structures the data for your traceability system , so you can demonstrate chain-of-custody in seconds during an FDA inspection rather than scrambling through paper files.
You define your acceptance criteria for each ingredient , chemical, physical, and microbiological parameters. Customiser compares each supplier spec sheet against those requirements and flags deviations, ensuring only compliant ingredients are approved for use in production and preventing the out-of-spec materials that cause batch holds and rework.
Food and beverage companies achieve 300-500% ROI within 18-30 months of implementing document automation, driven by reduced manual labor, faster batch release cycles, fewer audit findings, and avoidance of recall costs , the average food recall costs $10 million in direct expenses. Customiser reduces document processing time from hours to minutes per batch while helping reduce food safety incidents by up to 75%.
Yes. Customiser's AI extraction agents leverage multilingual capabilities to parse, translate, and extract structured data from documents regardless of source language. The extraction output is standardized into your chosen language and schema, meaning your QA team reviews consistent results whether the source document was in Japanese, Portuguese, German, or any other language.
Customiser creates a continuously updated, searchable knowledge base of all processed documents with extracted metadata, meaning you can retrieve any supplier's CoA history, specification change log, or non-conformance record in seconds. Because extraction results are structured and timestamped, you can demonstrate systematic supplier verification controls , exactly what auditors want to see.

No manual reviewing.
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