Implementation Team
Work with specialists who learn your lab’s workflow, instruments, and compliance requirements from day one.
LIMS IQ
Full LIMS IQ platform
DOC LIMS-IQ
REV 2026-09
REV 2026-09
LIMS IQ: cloud LIS/LIMS platform for toxicology, molecular, public health, and multi-site labs
LIMS IQ is the full cloud LIS/LIMS platform for clinical, toxicology, molecular, public health, and multi-site laboratories, priced on monthly requisition volume with unlimited users. Configurations, HL7 and instrument interfaces, migrations, and ongoing optimization are designed around how your lab actually operates.
- Volume-Based Pricing
- Unlimited Users
- Multi-Site Profiles
- Custom Interfaces
Unlimited users
Bench, operations, billing, and leadership teams share one volume-priced subscription without per-seat fees.
Phased delivery
Discovery, configuration, interfaces, validation, training, and go-live move through defined readiness gates.
Room to scale
Multi-site profiles, optional modules, and volume tiers adapt as the lab's workflow grows.
Product view
When off-the-shelf options fail, we build with you—your trusted, long-term partner.
CUSTOMIZED BY DESIGN
We map your lab's processes end to end, then configure accessioning, reporting, billing, and analytics to match your exact requirements. Assigned specialists and deep discovery ensure the system fits your staff, compliance needs, and growth plans.
- Implementation Team
- Tailored Workflow Configuration
- Integration & Data Strategy
- Business-Aligned KPIs
- Ongoing Optimization
- Security & Compliance
Key Capabilities
6 capabilitiesExplore the core capabilities available for this laboratory workflow.
Tailored Workflow Configuration
Custom panels, routing rules, reference ranges, and report templates built for your operations.
Integration & Data Strategy
HL7/API integrations, data mapping, and migrations planned to reduce downtime and errors.
Business-Aligned KPIs
Analytics dashboards and quality metrics aligned to your leadership goals and regulatory reporting.
Ongoing Optimization
Assigned specialists for enhancements, change requests, and scaling as your lab grows.
Security & Compliance
Role-based access, audit trails, and validation support tailored to your risk profile.
Frequently asked questions
8 answers on file
Q01
What kind of customization is in scope for the full LIMS IQ platform?
The full platform supports tailored test catalogs, accessioning forms, reflex rules, auto-verification logic, report templates, label layouts, instrument interfaces, HL7 ORM/ORU/DFT mappings, and analytics dashboards. The team configures LIMS IQ around your actual workflow — clinical, toxicology, molecular, public-health, or mixed — rather than asking the lab to bend its operations to a fixed template.
Q02
How long does a full-platform implementation typically run?
Timelines depend on test menu complexity, instrument count, interface partners, and migration scope. A typical implementation runs through discovery, design, configuration, interface build, validation, parallel testing, and go-live in defined phases so the schedule is predictable. The team plans milestones up front instead of treating the project as open-ended.
Q03
What can lab administrators configure after go-live?
Lab administrators can use the self-service Compendium to add, adjust, or retire tests, panels, analytes, reference ranges, critical limits, sample types, containers, and units without custom coding. Reflex rules and report templates are configuration changes rather than contract changes, and larger additions such as new interfaces, sites, or workflows can be scoped with LIMS IQ support.
Q04
Can LIMS IQ migrate data from our existing LIS?
Yes. The implementation team plans data migration alongside the configuration effort — historical orders, results, patients, providers, and reference ranges can be mapped and loaded with validation passes before cutover. Migration scope is defined during discovery so the lab knows exactly what is being moved, what is being archived, and how legacy lookups will work after go-live.
Q05
How are CLIA, CAP, and HIPAA expectations handled in a custom build?
LIMS IQ configurations are built on platform controls that support CLIA, CAP, and HIPAA requirements: role-based access, immutable audit trails, validated workflows, and versioned configuration changes. The implementation team works through validation documentation with the lab so the customized workflow is defensible during inspections and internal compliance reviews.
Q06
Can LIMS IQ run a multi-site lab network on one platform?
Yes. LIMS IQ manages multiple lab locations from a single platform with multi-site profiles: each location can run its own accessioning queues, instruments, and label and report templates while sharing one test catalog, user directory, and consolidated reporting across the network. Additional sites and multi-site profiles are scoped as the network grows rather than deployed as separate systems.
Q07
Which instruments and analyzers can connect to LIMS IQ?
LIMS IQ uses bidirectional ASTM and HL7 interfaces, plus custom and file-based patterns, to send worklists to chemistry, hematology, immunoassay, molecular, microbiology, and toxicology analyzers and receive results automatically. An instrument registry tracks each analyzer's calibration and QC status and the reagent lots loaded on it, so only validated instruments are available for use.
Q08
How are HL7 ORM, ORU, and DFT interfaces handled?
The built-in HL7 engine receives electronic orders (ORM) from EHRs such as Epic, Cerner, Allscripts, and Practice Fusion, returns verified results (ORU) to the ordering system, sends billing data (DFT) to downstream systems, and connects to reference labs such as LabCorp and Quest. Field mappings are configured per interface so each partner receives data in the shape it expects, and interfaces are added through configuration and scoping rather than custom code.
Related guides
Buyer's guides on the workflows this lab type runs- About LIMS IQ | Cloud LIS Software for Clinical Labs LIMS IQ is cloud LIS software for clinical and specialty labs, connecting accessioning, specimen tracking, instrument interfaces, reporting, and portals.
- Starting a Clinical Lab: CLIA, Instruments & LIS A sequenced checklist for starting a clinical laboratory: legal setup, CLIA certificate types and state licensure, lab director and personnel, space and instruments by test menu, LIS selection and interfaces, payer enrollment, QC and proficiency testing, and go-live.
- Cytogenetics & FISH LIS Software Cytogenetics and FISH LIS software: probe lot tracking, dual-technician scoring worksheets, ISCN result reporting, and combined molecular reporting.
Related resources
Expert guidance on workflows, compliance, and lab operations- LIMS IQ Named to CIO Bulletin's Best Companies to Watch 2026 CIO Bulletin included LIMS IQ in its Best Companies to Watch 2026 list, profiling the cloud-based LIS platform for modern clinical and specialty labs.
- Westgard Rules & Failed-QC Review Westgard rules and Levey-Jennings charts flag failed QC, alert result reviewers, and support documented sample holds under the lab's SOP.
- LIS Billing Integration: Cutting Claim Denials LIS billing integration reduces avoidable claim denials with eligibility checks, code validation, automated charge capture, and cleaner first-pass claims.
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