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.

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.

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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Contact the technology team

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