Support discrete data delivery and clinical workflow integration where required.
LabGx helps laboratories launch, customize, and scale pharmacogenomic reporting with speed, flexibility, and clinical confidence.

LabGx is a healthcare SaaS platform for pharmacogenomic interpretation, translation, report generation, and lab workflow enablement.
It helps laboratories move from genotype output to clinically meaningful reports through configurable templates, curated interpretation logic, and integration-ready data workflows.
For laboratories, LabGx reduces implementation friction, supports differentiated PGx services, and enables scalable reporting without requiring each lab to build its own interpretation infrastructure.
Six composable building blocks — onboarding, customization, interpretation, integrations, delivery, and scale — designed to fit how laboratories already work.
A guided path to help qualified labs move from setup to sample-report generation quickly.
Adapt report structure, branding, language, medication lists, genes, guideline preferences, and evidence thresholds.
Translate genomic data into prescribing insights using curated, clinically governed logic.
Work with existing laboratory operations, file formats, instrumentation outputs, and downstream systems.
Support discrete data delivery and clinical workflow integration where required.
Move from individual reports to scalable report generation with less manual work.

Import genotype files or connect through supported lab workflows.
Translate genetic results into medication-specific insights.
Select layout, language, evidence preferences, branding, and reporting logic.
Generate reports or route structured data into downstream clinical workflows.
Upload, interpret, configure, deliver — one governed pipeline, configurable end to end.
We’ll map LabGx to your LIS, sequencer pipeline, and reporting stack — and show a live sample run on your data model.