// ERP & MRP FOR REGULATED MANUFACTURING
The ERP that adapts to you,
not the other way around.
Aurantium unifies inventory, manufacturing, quality, scheduling, resource planning, and accounting into one traceable platform, built for batch manufacturers who answer to auditors, from pharma and supplements to food, beverage, and cosmetics.
From raw-material receipt to finished-goods release. Every lot, every step, every batch.
// ONE PLATFORM, MANY LOCATIONS
Built for the operations that get inspected.
If you make it by the batch, trace it by the lot, and have to prove it to an auditor, Aurantium fits. We started in pharma. The model runs the same across every quality-driven, recipe-based industry.
Pharmaceuticals
Drug product & API manufacturing
Nutraceuticals
Supplements & vitamins
Food & Beverage
Ingredients, blends & finished goods
Cosmetics
Personal care & formulation
Specialty Chemicals
Compounds, coatings & blends
Contract Manufacturing
CDMO / CMO & private label
// WHY TEAMS STAY
The opposite of your last ERP.
Fast where it was slow, flexible where it was rigid, and backed by people who actually pick up the phone.
Fast
Pages load now, not after a coffee break, and new hires are productive in days, not quarters.
Reliable
No mystery crashes mid-batch, no "just refresh" during a shipment. It's there when the floor is.
Easy to learn
Modern, uncluttered screens your back office and your operators actually like using.
Flexible
Custom fields, configurable forms, and roles bend to your process, with no change request to a vendor.
Validation-ready
We support your IQ, OQ, and PQ, so going live is inspection-ready, not a year of paperwork.
Transparent pricing
No per-seat games, no surprise module fees. Pricing that fits your operation, explained up front.
Attentive service
Talk to people who know the product and your account, not a ticket queue or a reseller.
In production today
Already running real regulated manufacturing every day, not a slide-deck promise.
“Best ERP for pharma development, manufacturing, and packaging on the market — and we’ve seen them all.”
Proven in regulated production at
// ONE PLATFORM
Seamless integration of critical business functions.
Most regulated manufacturers stitch together a finance system, manufacturing software, a warehouse platform, and a pile of spreadsheets. Aurantium replaces all of it. One data model, one audit trail, one source of truth.
Accounts Payable
Vendor invoices, payment runs, checks, 1099 & positive pay.
Accounts Receivable
Customers, invoices, cash receipts, deposits & key-offs.
General Ledger
Chart of accounts, cost centers, budgets, period closings.
Inventory
Lots, locations, pallets, allocations & physical counts.
Manufacturing
Formulas, jobs, process orders, labor tracking & production posting.
Resource Planning
Demand forecasting, lot sizing & supply/demand balancing.
Scheduling Board
Real-time drag-and-drop resource & equipment planning.
Orders
Sales orders, allocation & fulfillment tracking.
Quality & QC
Sampling, lot release, holds & quality-status control.
Purchasing
POs, multi-step receiving & invoice matching.
Reports
Parameterized reporting & analytics across every module.
Administration
Roles, permissions, sessions, record locks & audit.
Utilities & Labels
Form printing, location & shipment label generation.
EDI & Integrations
Trading-partner orders, ASNs & invoice exchange.
Documents
Batch records & PDF generation from live data.
Status & Monitoring
System health, print queues & live job status.
// RESOURCE PLANNING
Higher line utilization, fewer schedule surprises.
Drag an operation onto a machine and Aurantium cascades the whole queue, recalculating downstream phases, matching equipment by capability, and surfacing allocation status in real time, so the plant reschedules in seconds when reality changes.
- Trait-based equipment matching across your resources — Blender, Tablet Press, Coater, Packaging Line, and more
- Cascade rescheduling of dependent operations
- Live, color-coded material allocation
// LOT & BATCH TRACEABILITY
Recall-ready in minutes, not days.
Track a lot from receipt through manufacturing, QC, and shipment, with every gram accounted for. Potency, expiration, retest dates and full parentage travel with the material, and every quality-status change is signed and logged.
- Genealogy & sub-lot parentage
- Expiration & retest with FIFO shipment logic
- Quality holds, quarantine, allergen & restricted-material flags
// WHY TEAMS SWITCH
You shouldn't have to choose between compliance and sanity.
Legacy ERP made regulated manufacturers trade speed, flexibility, and usability for a checkbox that says "compliant." Aurantium gives you both.
Aurantium// WHAT IT CHANGES FOR THE BUSINESS
Built for the floor. Measured in the boardroom.
The same traceable system that runs production moves the numbers leadership watches, from working capital to release times to audit readiness.
Faster batch release
QC status, signatures, and records travel with the lot, so release becomes a review instead of a paper chase.
Lower inventory & working capital
Demand and supply balanced in one system instead of spreadsheets, so you carry what you need, not what you guessed.
Fewer deviations
Configurable workflows and enforced quality states keep work inside procedure by default.
Recall readiness
Forward and backward genealogy turns a mock recall into a query, not a week of digging.
Less planning labor
Live scheduling and resource planning replace the hours lost rebuilding plans by hand every week.
Shorter onboarding
Modern, uncluttered screens get new hires productive in days, blunting the cost of turnover on the floor.
// BUILT FOR REGULATED MANUFACTURING
Compliance isn't a module. It's the foundation.
Audit trails, signed formulas, record locking, and granular access control are wired through every transaction in the system, not bolted on after the fact.
Batch records & signed formulas
Configurable batch-record forms printed from live job data, with role-based signature requirements on every formula.
Immutable audit trail
Who changed what and when, across lots, formulas, postings, and quality status.
Record locking
Concurrent-edit protection keeps two operators from ever clobbering the same record.
Role-based access
Granular permissions with per-user and per-role override sets and access classes.
21 CFR Part 11
Audit trails, access control, authentication and signed formulas, mapped plainly to the FDA's electronic records rule.
Read the breakdown →Quality lifecycle
Available, hold, quarantine & release states gate movement, allocation, and shipping.
Validation support
IQ, OQ, and PQ support so qualifying the system is a guided process, not a solo project.
Recall readiness
Forward & backward lot genealogy turns a recall or mock-recall into a query, not a week-long fire drill.
Change control
Formulas are versioned with approval status, so nothing changes silently and every revision stays traceable.
// CONNECTED
Talks to the systems you already run.
EDI trading partners, payroll, banks, and label printers plug straight in, so the data you already depend on flows in and out, with no re-keying.
// IMPLEMENTATION
The part everyone fears, made transparent.
Discovery, data migration, validation, parallel run, go-live, and support. We've already moved a live regulated manufacturer off legacy ERP, and we'll show you exactly what the path looks like before you commit.
See Aurantium in action.
Book a live walkthrough and we'll run a sample product end to end: formula, batch record, scheduling, and release. Then talk through how it maps to your operation.