Manage the complete laboratory workflow, from patient intake and specimen collection to result verification, reporting, billing, and laboratory operations, within a single cloud-native platform.
Run the full diagnostic process on one platform. Every stage shares the same patient, order and specimen context: no re-keying, no disconnected tools, and a single source of truth from registration to billing.
Discipline-aware workflows across clinical and specialized testing.
Support routine and specialized chemistry testing workflows.
Manage hematology testing workflows and reporting.
Support microbiology workflows, susceptibility testing, and reporting.
Manage molecular testing and genomic reporting workflows.
Structured pathology reporting and review workflows.
Support cytology review and reporting processes.
Bring your analyzers into one automated pipeline, cut manual transcription, and keep the bench moving.
Connect laboratory instruments into a unified results pipeline.
Ingest analyzer output and route it through your validation rules.
Push pending work to instruments and reconcile results back automatically.
Drive collection, accessioning and testing from scannable identifiers.
Reduce manual transcription and re-keying across the bench.
Manage many analyzers across sections and sites from one place.
Consistency, accuracy and governance built into the workflow, not bolted on afterward.
Governed reference ranges with draft, approval and effective-dating.
Flag improbable changes against prior results before release.
Rule-driven add-on tests triggered automatically from results.
Detect critical values with acknowledgement and timed escalation.
Run QC with multi-rule evaluation and proficiency testing.
Capture root-cause and CAPA for rejections and QC events.
Tamper-evident activity history across the laboratory.
Identify and track specimens end to end with scannable labels.
Event-sourced custody transfers with accountability at each step.
Coordinate collection, assignment and routing for staff and field teams.
Freezer, rack and slot tracking for organized specimen storage.
Cold-chain excursion logging with severity and resolution.
Manage recollection requests through to completion.
Catalog-validated rejection with root-cause analysis.
Structured synoptic reporting, macroscopic and microscopic capture, cancer staging, and multi-tier review with co-signature, designed for the way pathology teams actually work.
Manage molecular and genomic testing workflows with structured variant reporting and standardized classification, ready for genomics-oriented laboratories.
Support cytology review and standardized reporting, including specimen adequacy and structured result capture.
Exchange orders and results using modern healthcare data standards.
Interface with hospital and clinical systems over established messaging.
Receive and triage electronic orders into a controlled queue.
Connect referring clinicians and provider systems to the lab.
Integrate with surrounding systems through secured APIs.
Connect branches and partners across a laboratory network.
Intelligence that supports your team's operations, not a substitute for clinical judgement.
Ask questions across your laboratory data and get sourced answers.
Surface bottlenecks, workload and trends across operations.
Assist staff through routine, repetitive laboratory tasks.
Anticipate turnaround-time risk before SLAs are breached.
Help draft and structure reports for review and approval.
Invoice patients with itemized, auditable charges.
Bill corporate and institutional accounts.
Submit claims and process payer remittances.
Track payments, refunds and receivables.
Understand revenue across lines, payers and sites.
Export financial reports for finance and reconciliation.
Designed to support healthcare compliance requirements and built with auditability and governance in mind.
Grant least-privilege access aligned to each role.
Maintain a defensible record of who did what, and when.
Govern how laboratory data is created, changed and retained.
Tie every meaningful action to an identifiable actor.
Built with patient data protection in mind.
Intake to billing on a single platform. No stitched-together tools.
Verification, reflex, delta checks and governance built in.
Run multiple branches and collection points from one system.
FHIR and HL7 connectivity for connected healthcare ecosystems.
Turnaround analytics, dashboards and AI-assisted insights.
Cloud-native foundation designed to grow with your laboratory.
A Laboratory Information System (LIS) is software that manages the laboratory's diagnostic workflow (patient and order data, specimens, testing, result verification, reporting and billing) in one place.
An LIS is oriented around clinical and diagnostic laboratories and patient-centric workflows (orders, results, reports). A LIMS is typically oriented around samples and research/industrial laboratories. Eruntar is a clinical/diagnostic LIS.
Yes. Eruntar is a cloud-native, multi-tenant Enterprise LIS designed for clinical, hospital, reference, histopathology and molecular diagnostics laboratories, including multi-site networks.
Yes. Eruntar is delivered as a cloud-native platform, so laboratories can operate without maintaining their own server infrastructure.
Yes. Eruntar supports analyzer integration with automated result processing and worklist distribution, including multi-instrument environments.
Yes. The platform can send worklists to instruments and ingest their results back into the laboratory workflow.
Yes. Eruntar provides structured histopathology reporting and multi-tier review workflows, including synoptic reporting and cancer staging.
Yes. Eruntar supports molecular and genomic testing workflows with structured variant reporting and standardized classification.
Yes. Eruntar supports microbiology workflows including susceptibility testing and reporting.
Yes. Eruntar supports cytology review and standardized reporting processes.
Yes. Both routine and specialized chemistry and hematology testing workflows are supported.
Yes. Eruntar supports multi-site laboratories with an organization, branch and collection-point model, so networks can operate many locations in one platform.
Eruntar supports reference and hospital laboratory operations across the full diagnostic workflow, with multi-site and network capabilities.
Yes. Eruntar supports HL7-based integration for exchanging orders and results with clinical systems.
Yes. Eruntar supports FHIR-based interoperability, including import and export of orders and results.
Yes. Electronic orders are received into a controlled holding queue for review before they enter the laboratory workflow.
Specimens are identified with barcodes and tracked across collection, accessioning, storage and testing, with chain-of-custody and rejection workflows.
Yes. Custody transfers are recorded as events with accountability at each step, suitable for sensitive specimen handling.
Yes. Cold-chain temperature excursions are logged with severity and a resolution workflow.
Eruntar provides turnaround-time analytics and predictive monitoring that surface risk before SLAs are breached, along with automation that reduces manual steps.
Reference-range governance, delta checks, reflex testing, critical-result monitoring, quality control programs, corrective-action tracking and audit trails.
Yes. Rule-driven reflex tests can be added automatically based on results, with execution traceability.
Yes. Critical values are detected and escalated with acknowledgement and timed follow-up.
Results move through multi-tier verification (technologist validation, pathologist review and final sign-off) with co-signature where required.
Reports can be delivered through multiple channels including email, SMS, messaging, portal and provider integrations, with delivery tracking.
Yes. Eruntar manages patient and corporate billing, insurance claims, payments, receivables, revenue analytics and financial reporting.
Yes. Eruntar offers AI-assisted operational intelligence such as knowledge search, operational insights, workflow assistance and reporting assistance, for operations support, not autonomous clinical decisions.
Eruntar is designed to support healthcare compliance requirements and is built with auditability and governance in mind, including role-based access and tamper-evident audit trails.
Yes. Access is governed by fine-grained, role- and capability-based controls so users only see what they should.
The Laboratory Module is currently in beta, and pricing will be announced at general availability. Beta access, including onboarding and migration support, is arranged through our team via the contact page.
Yes, as a beta. Laboratories can join the beta program to run Eruntar in production with close support from our team, and help shape the product before general availability.
The Laboratory Module is in beta. Pricing will be announced at general availability. Beta partners get early access, onboarding and migration support, and a direct line to the team building it.