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
06

Human validation

The final stage closes the analytical loop. Normal findings can be released quickly, while the system directs attention to the flagged cases. Following medical authorization, the reports are transmitted automatically back to the LIS.

Efficient release matrix and targeted expert focus

Mobiolink presents the validating physician or laboratory director with an aggregated overview of all measurement results. The system effectively separates routine operations from critical exceptions: standard findings, where all technical quality controls from previous stages remain valid, are grouped for rapid clearance. The expert's focus is instantly directed toward complex or borderline cases where curve kinetics, melting points, or control signals demand manual inspection.

Mobiolink interface: Val view — amplification curves (fluo/cycle) and well validation actions

Interactive curve analysis within the reporting dashboard

To support well-founded medical decisions, Mobiolink provides all relevant primary data directly within the validation workspace. The validator does not need to switch back to the instrument manufacturer's native software. With a single click, fluorescence curves, amplification trajectories, and historical patient data can be overlaid and displayed, allowing for a fast visual plausibility check directly on screen.

Complete documentation and audit trail

Every medical decision—whether it is a final release, an extraction repeat, or a manual result modification—is recorded in a tamper-proof manner within Mobiolink's audit trail. The system logs which user performed which validation step at what exact time, including any comments or justifications for exceptional releases. Every decision thus stays auditable and documented, supporting the lab's quality work.

Fully automated LIS ingestion

The moment medical authorization is granted, Mobiolink triggers the final data export. The interface translates the measurement metrics into the native protocol of the primary Laboratory Information System (LIS). Alongside the qualitative test result (positive/negative), quantitative values, specific Ct indices, and technical comments are transmitted in a structured format. This successfully closes the digital loop, making the report immediately available to the requesting physician.

Next Export of results to the LIS