NovoPath Clinical Pathology LIS
Your AP Lab Runs Clinical Work Too.
You Don't Need a Second LIS for It.
One
Patient record across
clinical and AP work
Direct
Analyzer interfaces,
no re-keying
99.9%
Uptime on cloud
infrastructure
Your AP Lab is Doing Clinical Work.
The Question is Whether the Software Knows.
Basic clinical testing is a natural extension of AP work. A biopsy patient also has a CBC. A GYN case comes with urinalysis. Chemistry panels support pathology diagnoses. And every one of those cross-specialty cases either lives in a single system or is stitched together by hand.
The labs that grow clinical work without growing overhead are the ones running both on the same platform, tied to the same patient record, using the same rules engine.
What We Hear from AP Labs Running Clinical Work.
Records Live in Two Systems
The AP LIS has one version of the patient. The clinical LIS has another. Reconciliation is manual, error-prone, and never quite finished.
Techs Are Re-Keying Analyzer Results
Chemistry and hematology instruments produce results. Techs type them into the LIS. Transcription errors happen. Turnaround slows.
Reflex Rules Live in Two Places
AP reflex logic is configured in one system. Clinical reflex rules are configured somewhere else. There is no single source of truth.
Inspection Prep is a Fire Drill
CLIA asks for QC control logs. Someone assembles them from the analyzers, the clinical LIS, and paper backups. It takes days.
NovoPath addresses all of this, not by adding complexity but by eliminating it.
One System. One Patient Record.
AP and Clinical Under the Same Roof.
One System, One Patient Record
Whether your lab combines clinical and AP orders on a single case or keeps them separate, NovoPath ties both to the same patient record. Your team isn't reconciling identity across two databases or toggling between platforms to see a patient's full picture.
Reflex Logic That Already Knows Your Rules
Clinical results run through the same reflex engine as your AP workflow. An abnormal chemistry result can automatically trigger the next appropriate test, without a tech having to catch it, look up the protocol, and place a manual order.
Results In, Without Re-Keying
NovoPath interfaces directly with your chemistry and hematology analyzers, so results post automatically instead of requiring manual transcription. Fewer manual entry points means fewer transcription errors and faster turnaround from instrument to report.
Every Feature of Our LIS Was
Built to Help Your AP Lab
Take On Clinical Work.
Auto-Release and Review Routing
Configurable rules auto-release results that meet your lab's criteria, so techs aren't manually signing off routine, in-range results one at a time. Anything outside those rules routes for review. Automation handles the volume, your team handles the judgment calls.
Batch Resulting
Verify and release multiple results in a single action instead of working case by case. When an instrument run produces a batch of results at once, your workflow can match it.
QC Capture
NovoPath captures instrument QC control data as part of the standard workflow, giving you a running record instead of a logbook to assemble before a survey.
Inspection-Ready Reports
QC control result logs, turnaround time by test and by day, and amended or corrected result reporting are available out of the box, along with the broader set of reports your lab needs for CLIA inspection readiness.

What Running Your Clinical Work
Feels Like With NovoPath.
AP Laboratory Running Clinical Testing
An AP lab running its clinical work on a separate system came to NovoPath looking to consolidate. Today, chemistry, hematology, and urinalysis run in the same platform as their pathology work, tied to the same patient record, with reflex logic shared across both. The team runs one lab instead of two, and inspection prep takes minutes instead of days.
Implementation Excellence:
Get It Right the First Time.
A successful transition begins with a structured, proven approach.
NovoPath will be on-site to see first-hand how your lab’s clinical work fits alongside your AP workflow. We’ll map your analyzer inventory, reflex rules, QC procedures, and CLIA reporting needs to scope the future-state buildout.
After reviewing your resources and current environment, NovoPath will deliver a workflow analysis and a phased configuration plan that fits your lab.
NovoPath will actively build the configurations required for your analyzer interfaces, auto-release rules, reflex logic, and reporting templates.
The team will conduct extensive testing and validation across every interface and every rule prior to final delivery. During delivery, we will work with you to issue the appropriate governances and permissions for your clinical and AP teams.
SME-led validation sessions with your laboratory stakeholders to ensure the system accurately reflects how clinical and AP work move together.
End-to-end testing of core workflows, including analyzer result posting, auto-release, reflex triggering, and QC capture in a controlled environment.
End-user training is conducted in parallel to ensure your team is confident before go-live.
Final production deployment of the validated system into the live laboratory environment. Real-time go-live monitoring with dedicated support resources available to resolve issues immediately as users transition into production workflows. Post-launch stabilization period focused on performance validation, user support, and rapid optimization to ensure full operational adoption and confidence.
300+
Labs Successfully Implemented
Almost without exception, labs that have made the switch tell us they wished they had done it sooner.
