Mobiolink
  1. Phase 1 LIS Requests received
  2. 01

    Intake & pre-sorting

    • Systematic processing and classification
    • Intelligent error and exception management
    • Guided pre-processing
    • Dynamic sorting logic and workflow optimization

    Clear steps – less manual work

  3. 02

    Extraction (RNA/DNA)

    • Structured batch generation and control spiking
    • Cycle of sequential process units
    • Provision of measurement-ready eluates

    Secure extraction – fully documented

  4. 03

    PCR setup (plate layout)

    • Strategic consolidation and flexibility (n:n logic)
    • Digital safeguarding and rule verification prior to execution
    • The core USP for PCR laboratories
    • Generation of precise physical operational instructions

    Flexible and controlled – optimal allocation

  5. 04

    Measurement (analyzer)

    • Seamless data import at the analytical device
    • Autonomous execution and optional real-time tracking
    • Structured data export as a trigger for downstream stages

    Clear processes – reliable results

  6. 05

    Automated result interpretation

    • Background ingestion and precise sample mapping
    • Algorithmic curve evaluation and Ct value calculation
    • Comprehensive technical validation
    • Automated release and proactive flagging

    Reliable interpretation – fast and consistent

  7. 06

    Human validation

    • Efficient release matrix and targeted expert focus
    • Interactive curve analysis within the reporting dashboard
    • Complete documentation and audit trail
    • Fully automated LIS ingestion

    Technical validation – focus on what matters

  8. 07

    Export of results to the LIS

    • Quality-driven export barrier and authorization concept
    • Intelligent method mapping and multi-LIS routing
    • Automated code conversion
    • Process transformation in daily laboratory operations

    Results correctly assigned

  9. Phase 2 LIS Validated results exported
Communication with the LIS Process within Mobiolink
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Export of results to the LIS

The final, highly secured data transfer to the LIS — fully controlled and rule-based. Results are transmitted only once all quality controls have been validated; method mapping and code conversion run fully automatically.

Quality-driven export barrier and authorization concept

A core protective principle secures the data transmission: as long as the quality controls (QC) of an assay are not fully validated and samples have not successfully passed technical validation, Mobiolink blocks the export. Incomplete or uncertain results are systemically prevented from reaching the LIS. As an additional layer of security, this functionality is tied to dedicated user permissions within the system's user management, natively fulfilling critical QM regulations.

Intelligent method mapping and multi-LIS routing

Mobiolink automatically cross-references measurement metrics with the originally requested LIS procedure. During export, this mapping occurs entirely in the background without requiring any manual selection or adjustment. If a laboratory or network is connected to multiple distinct LIS platforms, the software autonomously detects the target architecture and routes each result to the correct system without additional operational steps.

Automated code conversion

The system manages the complete bidirectional translation between internal laboratory assay codes and the specific target codes utilized by the LIS. All abbreviations, test designations, and units are adapted automatically. This consistent communication framework completely rules out translation errors or data inconsistencies between the platforms from the outset.

Process transformation in daily laboratory operations

From the perspective of the Laboratory Information System, Mobiolink interfaces smoothly like a single, standardized analytical instrument, making technical integration exceptionally straightforward. Because method-specific selections, mappings, and target system verifications are fully automated, the risk of incorrect data assignment is eliminated. Laboratory staff are liberated from administrative burdens, allowing them to focus entirely on analysis and medical validation.

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