Network rollup visibility without losing site-level ownership
For a health system, regional lab group, or multi-site POC program, the hard part is not only storing records. It is knowing which site is ready, which site needs attention, and where evidence lives when leadership, an accreditor, or a surveyor asks.
The verified product surface includes laboratory dashboards for personnel, test menu, instruments, QC activity, documents, PT, analytics, compliance reports, and organization-scoped records. The public Large Lab plan also lists unlimited personnel, locations, and instruments with enterprise reporting, audit trails, attestations, and advanced competency and training dashboards.
What leaders can centralize
- Personnel and competency status by lab or department.
- QC activity, investigations, and Levey-Jennings evidence.
- Document review, e-signature, and audit trail evidence.
- PT enrollment, reminders, performance review, and corrective actions.
- Equipment maintenance, calibration, and service history.
Readiness by accreditor: CLIA, CAP, COLA, and Joint Commission evidence
The product materials explicitly verify CLIA, CAP, and COLA readiness workflows, including a comprehensive CLIA/CAP/COLA survey prep dashboard in the Mid-Size Lab plan and related readiness pages for CLIA, CAP, and COLA.
CLIA
Track personnel qualifications, competency, QC, PT, validation, equipment, documents, and inspection readiness evidence tied to laboratory operations.
CAP
Use organized personnel, QC, Levey-Jennings, Westgard, documents, e-signatures, instrument, calibration, PT, validation, corrective action, dashboard, and reporting workflows for CAP readiness work.
COLA
Keep evidence organized across personnel, preanalytic, analytic, postanalytic, quality systems, procedure manual, facilities, safety, PT, QC, and test validation areas.
Joint Commission
Use the same evidence modules to map organization-specific requirements. This page does not claim a dedicated Joint Commission checklist module.
Waived and point-of-care testing at scale
Multi-site networks often need a common process for waived and point-of-care testing while still respecting local site ownership. myLabCompliance.io includes laboratory demographics, CLIA certificate management, laboratory type and specialty configuration, test menu management, FDA test classification resources, personnel and training workflows, QC schedules, equipment tracking, documents, and dashboards.
The public pricing data verifies urgent care as an intended audience for the Mid-Size Lab plan. For larger urgent care groups, hospital outpatient settings, or other POC networks, the enterprise conversation should focus on site count, instrument count, test menu scope, personnel roles, and which records must roll up to network quality leadership.
Document control and proficiency testing across sites
Documents
The existing site and app verify centralized document storage, version control, e-signatures, automated review cycles, audit trails, document categories, and signature request workflows. For enterprise teams, that means SOPs, policies, attestations, personnel documents, PT documents, and survey evidence can be managed in one place instead of separate binders and shared drives.
Proficiency testing
The feature set verifies PT program enrollment tracking, result submission management, performance analysis, corrective action documentation, calendar reminders, and PT document organization. Network quality leaders can use those workflows to keep PT follow-up visible across sites.
IT and procurement FAQ
What should we evaluate first?
Start with the number of CLIA sites, instruments, personnel, and required modules. The public plan data separates Small Lab, Mid-Size Lab, Large Lab, and Reference / High-Volume Lab by instrument volume and support needs.
Does the product publish enterprise pricing?
Public pricing lists Small Lab, Mid-Size Lab, Large Lab, and Reference / High-Volume Lab plans. Multi-site buyers should review the Large Lab and Reference / High-Volume Lab tiers and confirm fit during a demo.
Can IT discuss integrations?
Yes. The Reference / High-Volume Lab plan lists custom workflow automation and API integrations. Integration scope should be confirmed during procurement because each network's systems and implementation requirements differ.
Does myLabCompliance.io replace accreditor guidance?
No. The platform organizes compliance evidence and workflows. Your team should confirm accreditation requirements directly with the applicable accreditor and internal quality leadership.
Book an enterprise lab compliance demo
Bring your CLIA site count, accreditor mix, test menu scope, POC footprint, and current document/PT workflow. We will map the demo to the modules the product actually supports.
Book a demo