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    Cosmetics ERP

    ERP software for the cosmetic industry, compliant from batch to label.

    A single operating system for cosmetics brands, manufacturers and private label partners. Inventory, batch management, lot traceability and finance running on the same data model as your formulation and regulatory file, so a change at the bench reaches the label without re-keying.

    Quick answer

    ERP software for the cosmetic industry runs the operational backbone of a beauty business: raw material and finished goods inventory, supplier procurement, batch production, lot traceability, despatch and finance. A cosmetics-specific ERP also models multi-SKU, multi-country compliance, recall workflows under MoCRA and EU 1223/2009, and integration with formulation, PIF, CPSR and label artwork. Worldover delivers all of this on one platform, with formulation and regulatory in the same record rather than a separate system.

    • Multi-SKU, multi-brand, multi-site inventory and production
    • Lot genealogy from raw material lot to retailer pallet
    • Recall workflows that meet MoCRA and EU CPR expectations
    • Formulation and regulatory content on the same data model
    • Open integrations with 3PL, MES, LIMS, label artwork and finance
    • Built for brands, manufacturers and private label partners

    Why cosmetic operations are hard

    A cosmetics business is a substance business in operational drag. The portfolio runs to hundreds or thousands of SKUs across multiple brands, each formulated to different regulatory rules in every market it ships to. Raw materials have lots, expiries, retention samples and certificates of analysis that all need to travel with the batch. Finished goods are recalled by lot, not by SKU, which means the lot genealogy has to be live, not reconstructed.

    On top of that, regulation moves. A new SVHC addition, a revised Annex III concentration limit, a MoCRA guidance update or a Chinese NMPA change can make a formula and therefore a batch and therefore a label non-compliant overnight. An ERP that does not know about the regulatory file cannot propagate that change to operations, so the regulatory team ends up chasing batches with email.

    ERP software for the cosmetic industry is the answer when it is built for the industry, not bent into shape from a generic mid-market ERP. The difference shows up at audit, at recall, and at launch.

    Core capabilities

    Inventory and batch management. Raw materials, semi-finished bulks, finished goods and components managed by lot, expiry and location. Multi-warehouse and multi-site with real-time stock. Production work orders that pull components by lot, capture deviations, and close the batch record electronically against ISO 22716 and MoCRA cGMP expectations.

    Lot traceability and recall readiness. Full genealogy from raw material lot through bulk and fill to the customer despatch line. A recall query that takes seconds, not days. Retention samples linked to batches, batch records linked to the formula version that was assessed, and the formula version linked to the PIF and CPSR that approved it.

    Procurement and supplier management. Supplier specs, CoAs and SDSs captured as structured data, not PDF attachments. Goods receipt QC linked to the spec, with automatic flagging of out-of-spec lots. Spend and price history per supplier and per material.

    Integration with regulatory content and formulation. The ERP shares its data model with the cosmetic formulation software and the regulatory file. A formula change updates the BOM. An ingredient restriction flags every affected batch. A label artwork update triggers a version on the next production run. No re-keying, no parallel spreadsheets.

    Finance, despatch and customer. Sales orders, despatch, EDI to retailers and 3PLs, invoicing and an open API into the corporate finance ledger (Xero, NetSuite, SAP, Dynamics) if you would rather keep the books elsewhere.

    Designed for compliance-heavy cosmetics

    The platform is built so regulatory updates feed into operations as a first-class workflow, not a quarterly content release. Regulator feeds from ECHA, MHRA, FDA, NMPA and MHLW are ingested into the substance master. When a substance moves on Annex II, III or VI, when a new SVHC is added, or when MoCRA guidance changes, every affected formula, batch, label and notification is flagged automatically.

    That means the regulatory lead does not have to email the production manager to halt a batch. The batch flags itself. The CPSR refresh queues. The CPNP or SCPN notification update drafts. The label artwork team gets the new INCI list. The recall workflow is already armed with the lot list, should it come to that.

    See the cosmetic compliance software buyer's guide and the ERP vs PLM vs compliance explainer for the wider context.

    Worldover for this

    See Worldover for cosmetics ERP

    Operations, formulation and regulatory in one platform, built for the cosmetic industry.

    Explore the platform

    For manufacturers, brand owners and private label partners

    Cosmetic manufacturers and CMOs. Multi-customer, multi-brand production with customer-specific specs, regulatory ownership models (manufacturer-held vs brand-held PIF / responsible person), tolling workflows and the lot traceability customers will audit you on.

    Brand owners. A single operating system across in-house and contract-manufactured production, with the regulatory file owned in one place regardless of who makes the product. Direct line of sight into CMO batches, lot status and document compliance without a chain of spreadsheets.

    Private label partners. Manage hundreds of customer variants of base formulations, with customer-specific INCI ordering, claims, labels and notifications generated automatically from the parent formula. The platform tracks which customers received which version, and when their next notification update is due.

    The Iconic London case study is a worked example of a fast-growing brand consolidating operations and regulatory on one platform.

    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. 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
    Substance OS·one record, every module
    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...

    Meet Willow

    The AI connective tissue that flows through the entire operating system.

    Meet Willow

    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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