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A configurable laboratory information system

Moon LIS: Advanced Laboratory Information System

Moon LIS organises orders, specimens, results, verification and reporting in one workflow. Analyzer interfacing, barcodes, quality records and national-platform integrations can be scoped after reviewing each laboratory’s devices, protocols and actual operating process.

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The short answer

The system supports work from patient and order registration through barcode printing, specimen status, result receipt or entry, verification and report issue. Connecting an analyzer or platform such as NPHIES or Fatoora requires an interface scope, credentials, a test environment and technical acceptance by relevant parties; compatibility should not be assumed before testing.

Live Moon LIS Interactive Simulation

Interactive Moon LIS Workflow & Interface Preview

Explore the live laboratory workflow from barcode accessioning to clinical sign-off and national health integrations

Moon LIS Medical Core — Clinical Operations Station
Online: Riyadh Central Cloud Cluster | Latency: 18ms
#MOON-89241

Sample ID: #MOON-89241

Accessioned: 2026-09-16 08:42:15 | Specimen Type: Whole Blood EDTA + Serum Separator Gel

Active Routine Track
Patient Details Fahad Al-Saeed (Male, 48yo)
Medical Record (MRN) MRN-5049281
Ordering Clinic Internal Medicine & Diabetes (Dr. A. Al-Sharif)
Requested Tests Routine Chemistry (Glucose, Renal) + CBC Differential
Completed

1. Accessioning & Labeling

08:45:10 — Barcode verified
Completed

2. In-Processing on Analyzer

08:58:33 — Aliquots loaded
Completed

3. Technical Validation

09:05:12 — Delta check verified
Approved

4. Clinical Sign-off

09:12:00 — Dr. N. Al-Ghamdi
Delta Check: Passed (Creatinine deviation < 4%) Passed

Creatinine variance is 3.3% compared to baseline test from 30 days ago (well within safe limit < 4%; no acute renal variance observed).

Panic Values: None detected None Detected

All quantitative parameters remain strictly within safe clinical limits; no immediate telephonic doctor notification required per CBAHI protocols.

Analyte Parameter Observed Result Unit Reference Range Status Connected Analyzer
Fasting Blood Glucose 104 mg/dL 70 – 110 Normal Roche Cobas 6000
Serum Creatinine 0.92 mg/dL 0.70 – 1.20 Normal Beckman AU5800
Hemoglobin (Hb) 14.8 g/dL 13.5 – 17.5 Normal Sysmex XN-1000
White Blood Cells (WBC) 6.4 10³/µL 4.0 – 11.0 Normal Sysmex XN-1000
Platelet Count 245 10³/µL 150 – 450 Normal Sysmex XN-1000

When can Moon LIS fit?

  • A laboratory replacing fragmented records with a traceable workflow.
  • A laboratory network controlling orders, specimens and results across sites.
  • A technical team planning analyzer, HIS, claims or e-invoicing interfaces.

Capabilities that can be demonstrated and tested

Patient and order registration

Create the order and connect patient, test, physician or referral data with roles and an audit trail.

Barcode specimen tracking

Print identifiers and follow collection, receipt, rejection and processing states at configured work points.

Analyzer interfacing

Assess ASTM, HL7 or vendor interfaces and test messages, codes and mappings for each instrument.

Result review and reporting

Verification, authorisation and issue workflows with change history, report templates and laboratory-approved delivery methods.

Quality-control records

Record control values, trends, Levey–Jennings charts and laboratory-defined review rules.

Integration layer

Scope HIS, NPHIES or Fatoora work against published requirements, credentials and available test processes.

Information needed before a technical demonstration

  • Workload, sites, departments, test catalogue and coding.
  • Analyzer manufacturers, models, interfaces and available vendor documents.
  • Current specimen flow, roles, verification rules and report process.
  • Target systems, interface owner and available test environment.

From demonstration to controlled operation

  1. Workflow discovery

    We map orders, specimens, results and exceptions instead of only copying current screens.

  2. Configure and test a model

    We set data, roles and templates and test realistic scenarios with the team.

  3. Implement interfaces and migration

    Each device or system is treated as a separate interface with mappings, tests and error logs.

  4. Go live and support

    A readiness list, training, support route and indicators guide the transition and early operation.

Request a demonstration based on your analyzers

Send the analyzer list, site count, daily workload and target systems. We will distinguish what can be shown directly from what requires interface study or additional testing.

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Specialized Laboratory IT Guides & Healthcare Case Studies

Explore actionable technical resources on clinical laboratory digitalization, CBAHI accreditation, and NPHIES integrations:

Free Interactive Tool

Clinical Laboratory IT Readiness & System-Fit Adviser

Assess your lab's digital maturity, bidirectional analyzer interfacing, and national compliance readiness in minutes.

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Selection Guide

Selecting a Modern Laboratory Information System (LIS) in KSA

Core technical requirements for bidirectional interfacing, barcode accessioning, and delta check automation.

Read Complete Guide
CBAHI Standards

Digital CBAHI Compliance & Quality Control Automation

Implementing Levey-Jennings QC charts and Westgard multi-rules to ensure audit-ready accreditation.

Read Complete Guide
National Integration

NPHIES Platform Real-Time Insurance & Claims Integration

Automating electronic pre-authorizations and reducing healthcare claim rejection rates in Saudi Arabia.

Read Complete Guide

Contact the technology team

Select the system, number of sites and main operational issue. Your enquiry will go to the technology team.