End-to-End Sample Lifecycle
From request and registration through receipt, analysis, review, publication and disposal - one continuous, traceable flow.
A modern, configurable Laboratory Information Management System built for regulated laboratories. Streamline operations, ensure data integrity, and accelerate quality outcomes-end to end.
WHY XELLABS
Unify your lab's lifecycle from intake to disposal. XELLABS delivers an all-in-one, highly adaptable platform engineered for total compliance and effortless tool integration.
Comprehensive capabilities, from sample registration to analytics, powered by a single configurable, audit-ready core.
XELLABS gets your lab live fast - regulatory profile pre-configured, team onboarded.
Share your lab type, volume, and compliance needs. In just 30 minutes, we align you with the right configuration for your operations.
Your secure, dedicated environment is provisioned — pre-configured with roles, regulatory standards, and ready-to-use templates.
Quickly set up your products, test methods, specifications, and instruments. Import your existing data or configure it with guided support to ensure everything is audit-ready.
Start operating immediately with built-in compliance, real-time audit trails, and ready-to-generate reports — no delays, no complexity.
XELLABS ships with vertical configuration profiles and strong baseline capabilities. Switch profiles, not platforms.


Soil, plant tissue, fertilizer, feed, seed and pesticide samples; profiles; season/project batches; specifications; calculations; reports.
Water, wastewater, soil, sludge and air-related samples; preservation; holding times; custody; QC; compliance reports.
Raw material, in-process, finished product, environmental swab and shelf-life testing; specs; batches; COA.
Raw material, in-process, finished product and stability testing; specifications; worksheets; review; auditability.
Product, batch, blend, physical and chemical testing; formulas; specifications; certificates and trend data.
Projects, clients, studies, batches, flexible tests, sample partitions, reports and portal collaboration.
Sample intake, potency/contaminant panels, batches, QC, calculations, COA and client reporting.
Accessioning, aliquots, testing, verification, reference ranges, reports, audit and interfaces.
Controlled intake, custody, assignments, testing, QC, review, reporting, inspection access and audit history.
Tell us your lab type, compliance requirements, and current workflow. We'll tailor a focused 30-minute walkthrough - no generic demos, no sales pressure.
Fill in the details below and we'll reach out to schedule.
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