Worldover, AI operating system for substance-based businesses

    Chemicals · SDS authoring

    SDS authoring for chemical ingredient providers

    SDS authoring for chemical ingredient providers. Generate region-correct safety data sheets per substance and market from one record, and answer customer document requests without rebuilding the file.

    Today

    A customer asks for a safety data sheet in a language and format you don't hold, and the technical team spends a day rebuilding a document that already exists in another version.

    Authoring tools treat each sheet as a separate document. Serving twenty markets means maintaining twenty files that all describe the same substance.

    With Worldover

    Worldover SDS authoring connects substance identity, classification, registration status and use descriptors to the market, language and customer asking for the document.

    One substance record produces every market version of the sheet, and a customer request is answered the same hour.

    What's in it

    What SDS authoringdoes inside Worldover.

    The operational outcomes come first. Open any area to inspect the underlying controls, records and technical detail.

    Standards and regimes

    GHS and CLP
    01SDS AuthoringAutomated multi-language SDS generation across GHS and regional standards.
    • SDS generation

      Automated Safety Data Sheet generation compliant with multiple GHS revisions and regional formats.

    • Multi-language support

      Generate SDSs in multiple languages using regulatory phrase libraries.

    • Multi-jurisdiction support

      EU CLP, UK GB CLP, US OSHA HCS and other regional standards.

    • Version control

      Full version history and change tracking on every SDS.

    One workflow, end to end

    A customer opens a new market

    The difference isn't another isolated tool. It's the same work running from one live record.

    Where work breaks

    Documents are per market, not per substance

    The same classification is keyed into twenty files, and a correction has to be made twenty times.

    Requests interrupt technical work

    Every customer document request pulls a specialist away from the work only they can do.

    Registration status lives elsewhere

    What's registered, at what tonnage and for what use sits apart from the document that has to reflect it.

    1. 01

      A customer asks whether you can supply an ingredient into South Korea, with documentation to match.

    2. 02

      Today: someone checks registration status, then authors a fresh document from an existing one.

    3. 03

      In Worldover: the substance record already carries identity, classification and registration status.

    4. 04

      The market version of the sheet generates in the required language and format.

    5. 05

      The request, the version issued and the customer are recorded together.

    With Worldover

    1. 1

      One substance, many versions

      Market versions are generated from the same record instead of maintained as separate documents.

    2. 2

      Classification is derived

      GHS and regional classification comes from composition and hazard data, with regulatory review before issue.

    3. 3

      Requests are self-serve

      Customers get the current version through a portal, with delivery recorded, rather than by email chase.

    4. 4

      Change propagates

      A registration or classification update flags every market version and every customer holding an old one.

    Connected inside Worldover

    One product workflow.Every consequence connected.

    You sell substances, so the substance is the record. Everything a customer asks for, from the sheet to the declaration, is a view of it.

    Willow

    Useful AI starts with live operational context.

    Scoped permissions, human approval for anything material and a full audit trail of every action.

    • Which market versions of this SDS are out of date?
    • Which customers asked for documentation we haven't issued yet?
    • What's our registration status for this substance in South Korea?

    Buyer confidence

    A specialist system, without a specialist-system rollout.

    Worldover combines detailed operational control with a practical route to a live first phase.

    50+
    Enterprise customers across cosmetics, chemicals and supplements
    4 to 7
    Point systems typically retired, most within 6 months of go-live
    12 to 16 weeks
    To a live Phase 1, not a multi-year programme
    1 record
    Per substance, everywhere it appears

    See it on your operation

    See SDS generated from the substance record

    Give us the essentials, then choose a 30-minute slot directly in the right person’s calendar. We’ll use your workflow, products and documents, not a generic slide deck.

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