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Industry · Pharma
API and excipient specifications, ICH guidelines, cGMP and GDP frameworks, EMA, MHRA and FDA submissions. Worldover gives pharmaceutical teams an AI-native operating layer that respects every regulatory boundary by design.
USED BY 250+ INDUSTRY LEADERS
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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.
Validated systems take 18 months to deploy and are rigid the day they go live
CAPAs and deviations are paper-based, then re-keyed into multiple systems
Submission dossiers are stitched together from drives at the last minute
Each market's health authority has different document templates and timelines
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.
08:15 · An EMA variation guideline update is published. Willow identifies 9 marketed products in scope and drafts the variation strategy.
10:00 · A stability batch fails specification. The quality agent opens an OOS investigation, pulls all related batch and analytical records, and pre-drafts the deviation.
12:30 · A new CMO submits a batch record for review. The MES agent flags 3 procedural deviations against the approved master.
15:00 · A regulatory query lands from MHRA. The submission agent assembles the response with cross-references in 4 minutes.
17:00 · End-of-day digest: 14 deviations triaged, 3 CAPAs progressed, 0 overdue actions across the live product portfolio.
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 pharma, kept current automatically. No more chasing the latest update across PDFs and email chains.
GxP-ready
Built for validated environments from day one
1 record
Designed to keep CMC, quality and submission data in lockstep
Faster cycles
Designed to compress deviation, CAPA and submission timelines
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.
Compared against
If you're evaluating other tools alongside Worldover, these comparisons lay out what each system was built for and where each one fits.
Want to see how Worldover would deploy in your specific environment?
Talk to the team