The lab runs on LabMaster.
A clinical-grade Laboratory Information Management System for hospitals and diagnostic laboratories — sample registration through validated report, on a compliance-first architecture aligned with HIPAA, 21 CFR Part 11 and CLIA/CAP.
Deploys as managed SaaS, a dedicated instance, or fully on-premise.
Every specimen, traced from registration to validated result.
Built for the bench, not the demo stage
A laboratory lives or dies by traceability. LabMaster carries every specimen through the full chain — registration, accessioning, worklist, instrument result, quality control, supervisor validation, and signed report — with an audit trail behind every state change.
It is engineered the way regulated software has to be engineered: row-level data isolation, role-based access, clinical policy rules, and validation artefacts you can hand to an auditor. No shortcuts hidden under a polished screen.
Illustrative interface — a guided demo shows your own workflow.
What LabMaster does
Enterprise laboratory workflows, hybrid security, and interoperability — the four pillars the system was designed around.
Sample & Accession Management
Register, barcode and track specimens from collection to disposal. Chain-of-custody and specimen state captured at every hand-off.
Results & Reporting
Structured result entry with reference ranges and flags, supervisor validation, and clean, signed reports ready for the clinician.
Quality Control
QC runs, Levey-Jennings-style monitoring and rule-based holds keep out-of-control results off patient reports.
Audit Trails & Traceability
Every create, change and approval is recorded with user, timestamp and reason — the backbone of a 21 CFR Part 11-aligned record.
Hybrid Security
Row-level isolation, role-based access control and clinical policy rules layered together — tenant data stays tenant data.
Interoperability
FHIR R4 and HL7 / ASTM integration pathways for analysers, hospital information systems and electronic medical records.
Engineered for compliance — honest about certification
LabMaster is built compliance-first: its architecture is aligned with HIPAA, 21 CFR Part 11 and CLIA / CAP, and it ships validation-ready with IQ/OQ/PQ templates, traceability and standard operating procedures.
Certification is earned per deployment, with your quality team and your auditor — no software vendor can hand you a pre-issued certificate for your environment. What LabMaster gives you is the toolkit and the evidence trail to get there without rebuilding from scratch.
IQ / OQ / PQ templates
Installation, operational and performance qualification documents ready to execute.
Traceability matrix
Requirements mapped to controls and tests, end to end.
SOP library
Standard operating procedures aligned to CLIA / CAP expectations.
Electronic records & signatures
Audit trails and signature controls modelled on 21 CFR Part 11.
Deploy it your way
Same software, three footprints. Your data lives where your governance says it should.
Managed SaaS
We host, patch, monitor and back it up. You log in and run the lab. Fastest path to live.
Dedicated instance
Your own isolated environment in the region you choose — for tighter data-governance requirements.
On-premise
Runs on your own hardware via Docker Compose — for labs that keep everything inside the building.
Who it’s for
Hospital laboratories
Integrated with the hospital’s patient and order flow.
Standalone diagnostic labs
Walk-in and referral testing, billing-ready reports.
Multi-site lab networks
Many branches, one isolated record per tenant.
Research laboratories
Traceable workflows and exportable, structured data.
Request a guided LabMaster demo
Tell us a little about your lab and we’ll walk you through LabMaster on your own workflow — not a generic slide deck.
Your information is secure and never shared.
Frequently Asked Questions
See LabMaster on your own workflow
A guided demo, a scoped pilot, or a straight conversation — whichever suits your lab.