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QAM.Net

Audit Management Software

Plan, perform, manage, and coordinate your audits.
Simplified audit creation
thanks to AI assistant
Location & device-independent
audit acquisition
Automated scheduling &
action tracking

Audit Management Software QAM.Net
Audit Management Software QAM.Net

Always Be Audit Ready

The audit management software QAM.Net supports you throughout the planning, execution, and evaluation of audits. Based on freely definable questionnaires, the software allows you to model any process, product specification, or system detail of your company or area of responsibility and perform audit management in compliance with ISO 19011.

The software contains a variety of fully integrated questionnaires for pertinent standards and regulations. Whether ISO 9001, ISO 13485, IATF 16949, VDA, IFS, EMAS, VDA ISA 6.0 (TISAX), OHSAS occupational safety, or environmental management –QAM.Net allows you to use a software that was crafted with industry-specific quality requirements in mind and consistently facilitates standard-compliant audit planning and execution.

Functions of the Audit Management Software

  • Audit matrix
    Visualize the planning and implementation status of your audits using target/actual comparisons.
  • AI Assistant
    Let the integrated AI assistant support you with the creation of audit catalogues.
  • Wizard-led audit registration
    Use the audit wizard for simplified registration of first audits, follow-up audits or audits for multiple suppliers.
  • Question catalogues and checklists
    Whether predefined or individually created – the question catalogues and checklists in the software can be adapted to the respective requirements.
  • Individual schemes
    Whether random questions or random auditors – create your own need-based schemes.
  • Import & export audit catalogues and checklists
    If you have your own catalogues in Excel format or as an MDB file, for example, we can import them.
  • Direct access to relevant information
    You can view relevant documents, comments or objects directly in the audit.
  • Mobile offline audit processing
    You can acquire audits, a.o. via smartphone, tablet or laptop.
  • Processing of all audit types
    Whether system audit, product audit, process audit (also according to VDA 6.3) – all audit types can be implemented within the software.
  • Layered Process Audit (LPA)
    In the spirit of LPA software, QAM.Net supports you in establishing layered process audits (LPAs) in your company.
  • Connection to web portals
    You can exchange and process audits, such as supplier audits and supplier self-assessments via connected web portals, e.g. qxhub.
  • Audit acquisition
    When acquiring audits, you have the possibility to utilize visualization types, such as lists or turtle diagrams.
  • Audit annual planning
    With the graphical planning function you always have an overview of the audit schedule.
  • Findings & Actions
    Create findings directly during audit acquisition, analyze the corresponding root causes and define the necessary actions.
  • Action tracking
    You can control, delegate and monitor all actions resulting from an audit thanks to integrated action management.
  • Audit assessment
    Define your own evaluation scheme and scoring system for evaluating audits.
  • Audit evaluation & records
    Use predefined standard-compliant or individually adaptable calculations for evaluating audits and generate the respective records.

  • Mobile Audit Acquisition via Smartphone App

    The additional audit acquisition app provides you with access to all audits contained in the software QAM.Net and allows you to e.g. download them for offline acquisition purposes. The app is available in the App Store as well as in the Google Play Store and connection to QAM.Net is facilitated via CAQ.Net’s OpenAPI interface.

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Cross-Modular Functions

Standards-Compliance of the Audit Management Software

  • DIN EN ISO 9001
  • DIN EN ISO 19011
  • VDA 6.1, 6.2, 6.3, 6.4
  • IATF 16949
  • DIN EN ISO 13485
  • DIN EN 9100
  • DIN EN ISO/IEC 17025
  • DIN EN ISO/IEC 17021
  • FDA 21 CFR Part 820.22
  • GMP
  • IFS
  • More Regulations »
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