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    For your role

    Worldover for the Regulatory Affairs Manager in chemicals.

    Chemical regulatory work is a moving target. REACH dossiers, SVHC updates, CLP re-classifications, SDS in fifteen languages, poison centre notifications with UFIs, biocides and cosmetics ingredient files feeding back into brand customers. Every customer wants a slightly different SDS in a slightly different format, and every annex update ripples into hundreds of substances. Worldover puts the substance model at the centre, so REACH, CLP, GHS and downstream customer documents all read from one truth, and Willow drafts what your team used to type.

    Quick answer

    Chemical regulatory affairs software helps a Regulatory Affairs Manager run REACH registration and updates, CLP classification and labelling, GHS-compliant SDS authoring in every required language, poison centre notification with UFI, biocides files and customer-specific documentation. Worldover consolidates all of it on a substance-first data model with Willow drafting from live composition. Typical outcomes: 40 to 60% reduction in SDS authoring time, near-zero missed re-issues after CLP annex updates, and customer documentation packs generated on shipment instead of on request.

    • One substance record drives REACH, CLP, SDS, PCN and customer docs
    • Willow drafts SDS in every required language, reviewed in-system
    • CLP and SVHC annex updates surface affected products automatically
    • Poison centre notifications with UFI generation and per-market variants
    • Customer-specific SDS templates without duplicating source data
    • 40 to 60% less time spent on SDS authoring and reissue

    Who this is for, and who it is not for

    Built for: Regulatory Affairs Managers at specialty chemical manufacturers, ingredient suppliers and distributors handling 50+ substances across two or more markets, with real SDS authoring load and customer documentation obligations.

    Not the right fit for: single-substance producers with no downstream mixture work, or teams that fully outsource SDS authoring to a service and don't want to bring it in-house.

    If this sounds like you

    • You maintain SDS in a specialist tool that nobody else in the business can read.
    • Every CLP annex update triggers a manual sweep to find affected products.
    • Customers ask for SDS in their own template, and it takes days to reissue.
    • Poison centre submissions across EU member states are still partly manual.
    • You can't quickly answer "which of our mixtures contain this substance?"

    One substance, one truth

    Every substance has one master record: identity, composition, hazard classification, physical-chemical properties, toxicology and ecotoxicology, REACH status, regulatory annex flags. Every mixture inherits from its substances. Every SDS, label and notification reads from that record. Change the classification once, everything downstream updates.

    Worldover for this

    Bring one substance and see the whole chain

    Pick one substance from your portfolio, ideally one with EU + UK + US exposure. In 20 minutes a Worldover regulatory lead will walk it end to end: REACH position, CLP classification, GHS SDS in three languages, poison centre notification with UFI, and how a hypothetical CLP annex change would ripple into every affected mixture. You leave with a clear picture of the manual work this removes.

    Book a chemicals demo

    SDS authoring at scale

    Willow drafts GHS-compliant SDS in every required language from the mixture composition and its substances' hazard data. The regulatory manager reviews, questions, approves. Section 15 pulls from the live regulatory map (REACH, TSCA, DSL, IECSC, K-REACH, etc). Customer-specific templates apply without duplicating source data.

    CLP, SVHC and annex monitoring

    Willow monitors ECHA annex updates, SVHC list changes, ATP publications and equivalent feeds. When a substance's classification or status changes, every affected mixture surfaces in the queue with the required action: reclassify, reissue SDS, update label, re-notify poison centre. No manual mapping.

    Poison centre notifications

    Worldover generates PCN dossiers with UFIs per market, tracks submission status across ECHA and national portals, and re-issues when composition or classification changes. UFIs are managed on the mixture record and printed on the label automatically.

    Customer documentation without the fire drill

    Every shipment can carry the customer-specific pack: SDS in the customer's language and template, TDS, CoA, REACH declaration, RoHS statement, conflict minerals response. Generated on shipment, delivered with the goods, logged for audit.

    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
    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
    Where is Citral exposed across supply and demand?
    Ask Willow anything...

    The backstory

    What actually is Worldover?

    Worldover began life as a PLM, formulation and compliance tool, focused on giving the chemical and cosmetics industries the enterprise software they always needed.

    Success here led us to a bigger realisation. Yes, substance-based businesses needed better software, like Worldover. But they also needed less software. They wanted one system: a true operational nucleus. A system of record with a foundational data layer designed for substances – one that understands formulations, regulations, raw materials and ingredients. A central hub that replaces the patchwork of point tools holding teams back in regulated industries, whilst threading powerful, contextual AI throughout.

    That’s what Worldover is today.

    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.

    By submitting you agree to be contacted by Worldover. We'll never share your details.