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    Solution · Food safety

    HACCP software that lives inside production.

    A HACCP plan written in a document and monitored on a clipboard is two systems that disagree by lunchtime. Worldover holds the hazard analysis, the critical control points and the monitoring records against the same production batches they govern, so verification evidence exists without anyone assembling it.

    Quick answer

    HACCP software manages a Hazard Analysis and Critical Control Point food safety system: the hazard analysis, the identified critical control points, critical limits, monitoring procedures, corrective actions, verification and record-keeping. Worldover runs the seven HACCP principles against live production data, so CCP readings are captured at the line, deviations open a corrective action automatically, and verification records are generated from the batch record rather than transcribed into it.

    • Hazard analysis linked to the actual ingredient and process record
    • CCPs with critical limits enforced at the point of capture
    • Deviations open a corrective action automatically
    • Verification and validation records generated, not transcribed
    • Links straight to lot traceability and recall scope
    • Audit pack produced on demand for BRCGS, SQF, FSSC 22000

    How this connects to Worldover

    Replacing five subscriptions with one system you actually run the business on?

    Worldover is the AI operating system for chemicals, cosmetics and supplement businesses. One platform, one data model, custom-built around each team.

    See how Worldover works

    The seven principles, and where software actually helps

    PrincipleWhat Worldover does
    1 · Hazard analysisHazards held against the ingredient and process step, inherited by every product that uses them, so a new supplier risk propagates instead of sitting in one document.
    2 · Determine CCPsCCPs defined on the process route, versioned, with the decision rationale attached.
    3 · Critical limitsLimits enforced at data entry. An out-of-spec reading cannot be quietly recorded as in-spec.
    4 · MonitoringReadings captured at the line, timestamped, attributed, tied to the batch and lot.
    5 · Corrective actionsA breach opens a CAPA, holds the affected lots and scopes the exposure automatically.
    6 · VerificationScheduled verification, calibration and review records with completion tracked, not assumed.
    7 · Record-keepingEvery record is the operational record, so the audit pack is a view rather than a rebuild.

    Where paper and spreadsheet HACCP breaks

    • Version drift. The plan is updated, the line is still working from a printed copy.
    • Retrospective completion. Readings filled in at the end of a shift, which auditors detect and regulators treat as no record at all.
    • Orphaned deviations. A CCP breach recorded but never linked to the lots it affected.
    • Ingredient changes. A supplier swap introduces an allergen and nobody reopens the hazard analysis.
    • Audit scramble. Two weeks of preparation to produce evidence that should have been continuously available.

    HACCP, HARPC and the US position

    US firms operating under FSMA's Preventive Controls rule work to a Food Safety Plan rather than a classical HACCP plan: hazard analysis, preventive controls, monitoring, corrective actions, verification and a supply-chain programme, overseen by a Preventive Controls Qualified Individual. The structure is close enough that one system serves both, which matters for anyone exporting into the US from a BRCGS or FSSC 22000 site. Worldover holds both frameworks against the same underlying data rather than duplicating the plan.

    Worldover for this

    One system for food safety and operations

    HACCP, traceability, quality and production on the same live record, with Willow AI drafting the evidence.

    See how Worldover works

    Willow AI in the workflow

    Willow drafts hazard analyses from the ingredient and process record, flags where a formulation or supplier change should trigger a plan review, summarises open deviations before an audit, and answers questions such as which batches ran while a CCP was out of tolerance. Every output cites the records it used.

    Who this fits

    Specialty food and ingredient manufacturers, nutraceutical and functional food producers, and contract manufacturers running food alongside cosmetics or supplements. Pairs directly with food traceability software and quality management.

    FAQs

    Common questions.

    See Worldover on your operation.

    A 20-minute working session. Your SKUs, your customers, your documentation. No slide deck.

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    Worldover, AI operating system for chemicals and cosmetics companies

    The AI operating system for substances.

    Worldover is one system that replaces your ERP, PLM, QMS, LIMS, regulatory tools and more – and uses AI to orchestrate every workflow, at enterprise level. Designed for chemical, cosmetic and substance-based businesses.

    • 100% deployment success rate
    • Live in 3 months
    • 16 native modules, one data model

    Used by industry leaders

    HUDA Beauty, Worldover customerICONIC London, Worldover customerThe White Company, Worldover customer
    WorldoverWorldover OS
    Portfolio · 4 sites · 24 markets
    + 1,186 more ingredients
    Substance record

    Citral

    CAS5392-40-5INCICitralEC226-394-6
    GHS07GHS09
    Stock on hand
    840 kg
    Reorder point
    200 kg
    Next batch
    RUN-4821 · 14 Aug
    • F-2214Rose Attar EDP45 kg18 Aug
    • F-2287Velvet Body Lotion22 kg22 Aug
    • F-2301Signature Shower Gel38 kg29 Aug
    Willow · your AI operator
    How's supply looking on Citral?
    Ask Willow across 1,190 ingredients...

    Why Worldover

    A version of this is playing out 
    in your business , right now.

    These aren't edge cases. They're the normal operating conditions for brands, contract manufacturers, ingredient suppliers and distributors across cosmetics, specialty chemicals, food and nutraceuticals.

    Cosmetics · regulatory change

    The preservative just changed concentration in three EU markets.

    A regulatory update changes the permitted concentration of a preservative in three EU markets, effective in eleven weeks. Your quality lead searches the ERP for every affected SKU, finds seventeen, but cannot be certain the list is complete because the ingredient sits under two different INCI names across formulation records. The reformulation log lives in a spreadsheet. The brief is in a shared drive. The batch record is in a different system. By Friday evening there is a draft impact assessment. Nobody has touched the actual compliance documentation.

    Specialty chemicals · SVHC query

    The customer wants an SVHC answer by tomorrow.

    A specialty chemical distributor has just received a customer query about a substance on the SVHC candidate list. Their response depends on knowing which of their current product lines contains that substance, at what concentrations, in which formulations sold to which customers, in which markets. That data exists in four separate places: an ERP, a product database, a SharePoint folder, and a sales CRM that nobody has fully updated since the last rep left. The distributor is not short of systems. It is short of one system the business actually runs on.

    Food · FSMA 204 audit

    The traceability audit is six weeks out.

    A food contract manufacturer has a FSMA 204 traceability audit in six weeks. The regulation requires Critical Tracking Events to be logged at every point in the supply chain from grower to processor. Their current system tracks finished goods by lot. It does not log the upstream ingredient journey at the level of granularity the regulation now demands. The gap is not a data problem. It is an architecture problem. The truth the business depends on is split across too many places to be trusted.

    Nutraceuticals · NSF certification

    The reformulation needs a documentation pack, now.

    A nutraceutical brand is reformulating a product to meet NSF certification requirements for a new retail partner. The process requires identity testing documentation for every raw material, a certificate of analysis for each lot, a stability protocol, and a revised label claim review. All of that information exists. None of it is in the same system. The product manager is spending three days assembling a documentation pack that a properly designed backbone would have produced in minutes.

    The real problem isn't regulation. It's that the work is spread across too many systems – without one shared operational backbone.

    The full essay walks through why substance-based businesses are uniquely hard to run, why existing software has failed to solve it, and what an AI operating system actually means for this industry.

    Read the full essay

    Worldover connects your product, customer and regulatory data into one system.

    Then Willow, our AI layer, tells you exactly what to do with it. One platform replaces the patchwork of tools keeping chemicals and cosmetics businesses in the past. Worldover becomes the central hub for your entire operation.

    ERP

    Finance, procurement, inventory and operations in one data model.

    PLM

    Formulation, specs, versioning and change control from concept to shelf.

    QMS

    CAPA, deviations, audits and supplier quality without disconnected modules.

    CRM

    Customer relationships, orders and commercial data tied to the product record.

    LIMS

    Testing, specifications, batch release and COA management in the same workflow.

    Regulatory tools

    Ingredient restrictions, registrations, notifications and global filing status in one view.

    Compliance tools

    REACH, GHS, CLP and other substance rules checked against your live product data.

    Document authors

    SDS, PIF, dossiers, CoA and labels generated from the same source of truth.

    Implementation

    Live in 3 months.

    1. 01

      Weeks 1 to 4

      Scoping and data model

      Map your systems and configure the foundational data model.

    2. 02

      Weeks 5 to 8

      Configuration and migration

      Build modules, migrate master data and run parallel testing.

    3. 03

      Weeks 9 to 12

      Training, testing, go-live

      Train your team, run final QA and go live with support coverage.

    Backed by the world's best investors

    Chalfen Ventures, Worldover investor
    Index Ventures, Worldover investor
    Entrepreneur First, Worldover investor

    Enterprise-grade security

    SOC 2 certified

    SOC 2 certified

    Independently audited controls for security, availability and confidentiality.

    Book a demo

    See Worldover in action today.

    Give us 30 minutes. We'll show you exactly how Worldover would deploy in your business, with your processes, your data and your guardrails.

    • A live tour of the platform and Willow
    • Custom modules mapped to your workflow
    • Typically replaces 4–7 point solutions

    We'll send a calendar link within one business day.

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