01 · Cosmetics
INCI databases, EU CPR and FDA MoCRA frameworks, CosIng and allergen lists, IFRA standards, SCCS safety opinions.
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How it works
Worldover understands the ontology of your business, fits your processes, and responsibly deploys AI across your workflows.
Willow, our AI agent, reasons across every module. It drafts submissions, reconciles data, and takes actions on your behalf, always with a human in the loop.
PLM, QMS, LIMS, ERP, scheduling and finance in a single platform, configured for substance-based operations. No more stitched-together point tools.
A unified data spine: substances, formulas, batches, suppliers and regulations. One source of truth that every module and Willow can read and write.
Meet Willow
The AI connective tissue that flows through the entire operating system.
The frameworks, registers and reference data your industry runs on are baked in from day one. You don't spend your first six months teaching the software what an INCI or a CAS number is.
01 · Cosmetics
INCI databases, EU CPR and FDA MoCRA frameworks, CosIng and allergen lists, IFRA standards, SCCS safety opinions.
Use our template library of 20+ software modules, PLM, ERP, R&D, Regulatory, FP&A and more, to get started. Our success team customises the rest to give you the perfect solution. Unify your existing systems into one, fill in the gaps, or replace tools that just aren't working.
Manage every product from concept to discontinuation in one connected record.
Run the operational backbone: orders, inventory, production, and finance in sync.
Track every customer, opportunity, and commercial conversation in one place.
Formulate, iterate, and scale new products with full traceability from bench to batch.
Orchestrate lab samples, tests, and results with audit-ready data integrity.
Capture experiments, methods, and observations in a structured, searchable record.
Model scenarios, track performance, and steer the business with live financial insight.
Keep every formula, claim, and market compliant as rules and regions evolve.
Automate the creation of fully customisable Safety Data Sheet modules.
Source raw materials, manage suppliers, and control spend from PO to delivery.
Close the loop on deviations, CAPAs, and change control with full audit history.
Execute production on the shop floor with real-time batch records and work orders.
Track incidents, exposures, and permits to keep people and sites safe and compliant.
Run the warehouse end-to-end, from receiving through putaway, picking, and dispatch.
Publish accurate, channel-ready product information to every customer and marketplace.
Follow every batch and raw material from supplier to shelf, forward and back.
Willow gives every sub-agent explicit guardrails: scoped permissions, human approval steps for anything material, and a full audit trail of every action. Your team is always in the loop, and always in control.
Every formula, ingredient and SKU in one living record.
"New CMR restriction on BHT. 8 SKUs affected, drafted replacement matrices from your approved RM library, ranked by cost and scalability."
Bulk, semi-finished and filled goods in lockstep.
"Reconciled 312 open orders against the fill schedule. 4 bulk batches short, rerouted fragrance blend 2088 to your Antwerp line."
Every brand, buyer and brief in one place.
"Logged 14 contacts from in-cosmetics Paris. Matched each to your target brand list and drafted follow-ups with relevant formulation samples."
A formulation chemist that never sleeps.
"Drafted 4 paraben-free candidates within your cost band and flagged the 2 most scalable at pilot volume."
Every sample, every test, audit-ready.
"Released 47 stability and micro results overnight. 2 out-of-spec batches quarantined and flagged to QA."
No trial stuck in a chemist's notebook.
"Structured 23 emulsion trials from last week's bench work. Cross-referenced 4 with prior viscosity and stability data."
Live margins, raw material volatility, decisions.
"Q2 margin 3.2% below plan, shea butter spot price spike. Modelled 3 recovery scenarios and impact on top-10 SKUs."
Every formula, every market, always current.
"EU CLP Annex VI update lands 14 May. 18 SKUs affected. Drafted INCI revisions and CPNP notifications for review."
From PO to COA, without the chasing.
"3 suppliers overdue on vegetable-grade glycerin. Issued reminders, lined up a qualified alternate at +2.1%, COA on file."
Every CAPA, audit and reminder moving.
"Circulated the latest CAPA reports and H&S reminders. No outstanding items."
Real-time batch records, no clipboards.
"Released bulk batch 88241 of shampoo base for filling 40 minutes ahead of schedule. Yield 98.6%, in-process checks logged."
Catches hazards before they become incidents.
"Isopropanol STEL breached for 3 minutes on Line 4. Incident logged, supervisor notified, root cause drafted."
Receiving to dispatch, hazmat to finished goods.
"Prioritised 12 pick lists by shelf life. 2 flammables staged in the wrong zone, relocated to hazmat aisle."
Channel-ready product data, everywhere.
"Syndicated 47 new SKUs to 9 distributor portals overnight. INCI lists translated, allergen declarations set."
Every gram of CO₂e, defensibly.
"Updated Scope 3 with Q1 RM supplier data. New fragrance SKU: 1.84 kg CO₂e/unit, -12% vs 2024 reference formula."
Every batch, supplier to shelf.
"Recall simulation on batch 77203, 1,240 units traced across 3 distributors in 6 minutes. Notifications pre-drafted."
Implementation
Weeks 1 to 4
We map your current systems, data flows, and operational requirements. You assign a project lead. We configure the foundational data model.
Weeks 5 to 8
We build your module configuration, migrate your master data, and run parallel testing against your current stack.
Weeks 9 to 12
Your team trains on the live environment. We run final QA. You go live with full support coverage.
12–18 months
Typical time to full consolidation
Start with the modules you need now. Retire surrounding tools at each renewal. No big bang required.
One platform, your timeline
Worldover is one platform covering ERP, LIMS, QMS, MES, PLM, PIM, WMS, CRM, regulatory, procurement, EHS and FP&A.
But we know it's hard to rip everything out on day one. So if you're tied into SAP, LabWare or a legacy MES for another renewal cycle, Worldover wraps around them, runs the rest, and you consolidate at your own pace.
Replace
Worldover ERP runs orders, inventory, production and finance natively. Most customers retire their legacy ERP within 18 months of go-live.
Or wrap
Locked into SAP for another renewal cycle? We sit on top, sync master data and post transactions back until you're ready to consolidate.
Replace
Worldover LIMS, ELN and QMS are native modules. Samples, tests, stability, CAPAs and audit trails live in the same record as the formula and the batch.
Or wrap
Keeping LabWare or Veeva for now? Two-way sync on samples, results and CAPAs. COAs flow into Worldover batch records automatically.
Replace
Worldover MES is paperless batch records, work orders and live shop-floor execution out of the box. Operators run the line on Worldover.
Or wrap
Existing MES you don't want to touch? Stream batch progress, scrap and yield into Worldover. We schedule and reconcile, the line stays put.
Replace
PLM, PIM, WMS, CRM, procurement, regulatory, EHS. All native Worldover modules, one data model, one login.
Or wrap
Anything we don't yet replace, or anything you're contractually stuck with, we integrate. REST, GraphQL, EDI, SFTP, flat-file. If it has an interface, we connect it.
Worldover ships sixteen native modules on one data model. No bolt-ons, no second database, no integration tax between modules.
REST, GraphQL, webhooks, EDI, SFTP, flat-file, SAML/OIDC SSO. If it has an interface, we connect it. If it doesn't, we build the adapter.
Start with the modules you need now. Retire surrounding tools at each renewal. Most customers reach a single-platform state inside 24 months.
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Book a demo
Give us 30 minutes. We'll show you exactly how Worldover would deploy in your business, with your processes, your data and your guardrails.