EKLIS.CLIENT REPORT
CLIENT REPORT ยท FOR REVIEW & CONFIRMATION

EKLIS โ€” a cloud LIS from requisition to reimbursement

EKLIS (working name) is a multi-tenant SaaS Laboratory Information System for US clinical laboratories โ€” physician office labs, independent clinical labs, and small reference labs. This report presents the complete plan for your review; the Confirmation page lists the decisions we ask you to approve.

$2.3โ€“4.5Bglobal LIS market, 2025 (scope-dependent)
7โ€“9% CAGRwith cloud LIS adoption up 36%
80โ€“90%of routine chemistry auto-releasable โ€” the core ROI lever
Aug 2024benchmark LABGEN folded into MEDFAR โ€” a lab-first vendor gap opens

Executive summary

POSITIONING

The lab-first cloud platform

Order entry, analyzer connectivity, auto-verification, and clean claims in one system โ€” live in days, priced per accession. LABGEN's breadth on a modern cloud architecture, with RCM as software instead of a service.

WHY NOW

A lab-first vendor gap

Benchmark competitor Comtron LABGEN was acquired by MEDFAR (an EMR company) in August 2024. Incumbents are single-tenant legacy architectures while labs move to the cloud. LigoLab and XIFIN proved the LIS + RCM single-platform economics.

STRATEGY

Parity, then leapfrog

Match LABGEN's capability breadth (portals, interfaces, billing hooks) on multi-tenant SaaS, then differentiate: FHIR APIs, mobile collection logistics, AI-assisted operations, and in-product inspection readiness.

What this report covers

01

Market & Competition

Segments, the LABGEN/MEDFAR benchmark, competitor field, business model.

02

Platform & Architecture

Decided stack, system shape, architecture principles, non-functional targets.

03

Laboratory Workflow

The requisition-to-reimbursement pipeline, specimen lifecycle, verification & QC.

04

Connectivity

Analyzers, EHRs, reference labs, payers โ€” standards and interface engine.

05

Modules & Features

The full module map, portals, features by audience, differentiators.

06

Security & Compliance

HIPAA, CLIA, CAP/COLA โ€” how compliance is engineered into the product.

07

Requirements & Roadmap

R1โ€“R4 requirement families and delivery phases P1โ€“P4 with exit gates.

08

Confirmation

Open decisions, risks, and the sign-off checklist โ€” what we need from you.

Functional detail โ€” screen by screen

Six deep-dive pages specifying each core function against what the benchmark solutions ship today.

F-01

Staff

Roles, CLIA personnel mapping, competency & credential tracking, security.

F-02

Schedule

Patient appointments, draw sites, phlebotomy routes, standing orders, maintenance.

F-03

Order

Order entry in depth: OOE, requisitions, reflex & add-ons, AOE, eligibility, ABN.

F-04

Result

Entry grids, verification, delta & critical handling, comments, amendments.

F-05

Report

Report formats, custom design, branding, delivery channels, reprint audit.

F-06

Statistics

KPI dashboards, TAT, volumes, productivity, financial & QC analytics.

How to review this report

Read the plan

Pages 01โ€“07 present the full plan: market case, architecture, workflow, connectivity, modules, compliance, and roadmap.

Note questions

Anything unclear or contested โ€” mark it. Every section maps to a source planning document we can drill into together.

Confirm decisions

The Confirmation page lists each open decision with our recommendation. Approve, amend, or defer each one.

Kick off P1

With confirmations in hand, Phase 1 (foundation & core loop) starts against the agreed scope and gates.