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    Solution · Distribution

    Distributor ERP software for substance-based portfolios.

    A distributor of regulated substances is not a warehouse with invoices attached. You inherit every supplier's regulatory obligations, re-author their documents under your own name, repack into your own lot codes, and answer customer questions your suppliers were slow to answer. Worldover runs that as one system instead of a warehouse system plus a compliance team plus an inbox.

    Quick answer

    Distributor ERP software manages purchasing, stock, repacking, pricing and fulfilment for distributors, and for distributors of chemicals, ingredients and cosmetic raw materials it must also manage regulatory obligations inherited from suppliers: SDS re-authoring under your own details, CLP and GHS labelling, REACH roles, poison centre notification for repacked mixtures, and customer documentation packs. Worldover holds the substance master once and generates the commercial and regulatory outputs from it.

    • Repacking with full lot genealogy from supplier lot to customer lot
    • SDS re-authored under your legal entity, per market and language
    • CLP, GHS and UFI handled for repacked mixtures
    • Customer documentation packs answered from live data
    • True margin per line, per customer, per substance
    • Supplier document ingestion with Willow AI extraction

    How this connects to Worldover

    Keeping SDS, REACH and CLP current across a growing substance master?

    Worldover holds the substance, mixture, SDS and label as one live record so REACH, CLP and multi-market SDS regenerate the moment the underlying data changes.

    See AI ERP for chemicals

    What generic distribution ERP misses

    Standard distribution ERPs model a product as a code with a price and a quantity. That works until the product is a substance. Then the code carries hazard classification, a supplier SDS that expires, exposure scenarios, a REACH role that changes depending on whether you repack, and customer declarations that must be answered within days.

    The usual result is a competent ERP surrounded by a compliance function operating entirely in documents, with a shared mailbox as the integration layer.

    Where distributor margin actually leaks

    • Documentation labour. Skilled staff re-typing supplier data into SDSs, TDSs and customer questionnaires.
    • Response lag. Deals lost because a customer's regulatory pack took nine days and a competitor's took one.
    • Repack costing. True cost per repacked lot rarely modelled, so small-volume lines quietly lose money.
    • Obsolete stock. Substances restricted or reclassified after purchase, discovered at sale rather than at listing.
    • Freight and hazard surcharges absorbed rather than recovered because they are not attached to the line.

    Repacking, and the regulatory consequences of it

    ActivityWhat it triggers
    Repack into own packagingSDS and label under your details, new lot code, genealogy back to the supplier lot.
    Blend or diluteNew mixture classification, new UFI, poison centre notification in each market of placement.
    Import into the EU or UKImporter duties under REACH and UK REACH, including registration or Only Representative arrangements.
    Supply into the USOSHA HazCom SDS format, TSCA inventory status for each substance supplied.
    Sell to cosmetics customersINCI data, allergen declarations, animal-testing statements, PIF-supporting documentation.

    Worldover for this

    One system for stock, documents and margin

    Purchasing, repacking, compliance and customer service on the same substance record.

    See how Worldover works

    Willow AI in the workflow

    Willow reads inbound supplier SDSs and specifications, extracts the classification and composition data, and flags where a supplier revision changes your own document set. It drafts the customer questionnaire response from live data, and answers commercial questions such as which customers bought a substance now facing restriction, and what that exposure is worth.

    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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