We use cookies to understand site performance and improve follow-up from our team.
Industry · Supplements
Botanical dossiers, EFSA and DSHEA frameworks, authorised health claims and GMP requirements. Worldover lets supplements brands and manufacturers move fast without burning the regulatory bridge behind them.
USED BY 250+ INDUSTRY LEADERS
Navigate by your business type
For contract and private label manufacturers managing complex formulations and shop floors.
For beauty, chemical, and FMCG brands driving global formulation compliance and launch speed.
For suppliers and developers of chemical substances, raw materials, and active ingredients.
For regulatory-focused chemical and cosmetics distributors overseeing multi-market supply chains.
Sound familiar?
These are the symptoms of a fragmented stack. Worldover replaces the lot.
Health claims on the website don't match the substantiation file
Reformulating to remove a contentious botanical takes weeks of cross-team work
Each manufacturer wants spec data in their own template
Dossiers and CoAs live in inboxes, never indexed when an auditor asks
A day in the life
AI workflows, coordinated by Willow, manage the tasks that slow your business down. Every action is logged, and every decision is yours to approve.
08:00 · EFSA updates an Article 13 list. Willow flags 4 active SKUs whose claims are now non-compliant and drafts replacement copy.
10:30 · A new pre-workout formulation is signed off. The compliance agent generates labels for EU, UK and US, each with the correct claim wording.
13:00 · A manufacturer submits a CoA. The QC agent reconciles it against your spec, flags one out-of-trend value, and notifies the buyer.
15:30 · A retailer asks for a substantiation file for a beauty-from-within claim. The regulatory agent assembles it from primary sources in 5 minutes.
17:00 · End-of-day digest: 23 health claims reviewed, 8 CoAs approved, 0 substantiation gaps across the live catalogue.
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.
Compliance, built in
Every framework that touches supplements, kept current automatically. No more chasing the latest update across PDFs and email chains.
Compliant claims
Built so every claim is traceable to authorised substantiation
Audit-ready
Designed to make CoAs, dossiers and batch evidence findable in seconds
Faster launches
Designed to compress regulatory and labelling cycles by market
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.
Software for supplements teams
Deploy the blocks supplements teams use most. Each one is part of the same operating system, so the formula, the regulation and the batch never disagree.
Chemical compliance software
Ingredient master, restricted-substance screening and customer declarations.
Explore solutionSDS authoring software
GHS-compliant, multilingual SDS authoring for nutraceutical ingredients.
Explore solutionChemical ERP software
Batch, lot traceability and supplier documentation in one ERP.
Explore solutionWant to see how Worldover would deploy in your specific environment?
Talk to the team