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    Early accessGeneral release planned for 2027Request access

    Laboratory software for testing, QC and research labs

    Lab journal, samples, QC, equipment and quality management on shared records

    LabNote.Light brings together the lab journal, samples, methods, equipment, quality management and safety documents. Evidence remains with each case from the work order through report release.

    • Shared master data for samples, methods and equipment
    • Review, signature and change history on the record
    • Introduce modules individually and use them together when needed

    Data stored in Frankfurt (AWS) · DPA under Art. 28 GDPR

    One laboratory order

    One order, traceable through release

    Drinking-water sample PB-2026-0184 shows how technical work and evidence stay together. Every step refers to its underlying record.

    1. 01

      Receive sample

      Order, due date, storage position and QR label stay with the sample.

      Details
    2. 02

      Assign method and equipment

      Test plan, method DIN EN ISO 10304-1 and IC-02 are linked.

      Details
    3. 03

      Check equipment evidence

      Calibration, maintenance and qualification stay in the equipment record.

      Details
    4. 04

      Verify result

      Entered values are reviewed separately; an OOS result blocks report release.

      Details
    5. 05

      Handle deviation

      Cause, action and effectiveness check remain connected as a CAPA.

      Details

    02 · Equipment evidence

    Calibration and qualification on the equipment record

    Due dates, certificates, measurement uncertainty and signed IQ/OQ/PQ evidence remain on the equipment record and are available to the test workflow.

    Equipment & calibration

    03 · Result review

    Entered values are not yet released results

    Specification, measurement uncertainty and decision rule are reviewed visibly. Open deviations can block report release.

    Methods & QC analytics

    04 · CAPA

    Keep deviation, action and effectiveness together

    A CAPA connects the original finding with root-cause analysis, ownership, due date and later effectiveness review.

    Documents, audits & CAPA

    Daily laboratory work

    Tasks, due dates and data exchange on the record

    Inbox, QR access, customer portal and interfaces complement the domain modules. The optional assistant can summarise content or suggest text. Users review these suggestions; approvals and technical decisions remain with the responsible people.

    • QR labels for samples, equipment and storage locations
    • Customer portal for status and released reports
    • REST API, webhooks and defined connectors

    Quality and evidence

    Workflows for ISO/IEC 17025 and ISO 9001

    LabNote.Light supports workflows under ISO/IEC 17025 and ISO 9001 — from contract review and methods through audit, CAPA and management review. Accreditation and certification concern the organisation and its operating processes, not the software alone.

    Adoption

    Start with the modules you need

    LabNote.Light is in early access. Pricing is per user from a minimum of ten users; plans differ in support, onboarding and storage.

    View pricing

    Common questions

    Do all modules need to be introduced at once?

    No. Modules can be used individually and connected later on the same data core.

    Is LabNote.Light certified to ISO/IEC 17025 or ISO 9001?

    No. The software supports documented workflows. Accreditation or certification assesses the laboratory or organisation.

    Does the assistant make technical decisions?

    No. Users must review suggestions and summaries. Approvals and signatures remain separate, person-bound steps.

    Review LabNote.Light against your workflows

    Early access is for laboratories that want to review their requirements directly with the product team.

    Request early access