QBD.Net

Document Management Software

Create, control, and manage your documents.
Always work with the latest
version
of the documents
Change tracking & monitoring
of control tasks
Document processing
e.g. with MS Office

Document Management Software QBD.Net
Document Management Software QBD.Net

Standard-Compliant & Paperless Document Management

Apart from guidelines regarding the document creation process, standards and specifications such as ISO 9001, IATF 16949, and ISO 13485 also contain detailed guidelines relating to the maintenance, control, and version management of documents. These requirements quickly exceed the limits of manual document management and make the use of a sophisticated software solution such as QBD.Net virtually unavoidable.

The document management software QBD.Net is fully embedded in your existing MS Office environment, allowing you to continue to work with the programs you are familiar with and use QBD.Net to control all document monitoring and maintenance processes. Amongst a host of other functions, the software includes sophisticated escalation management, rights management, electronic signatures, project tracking, and facilitates a 100% paper-free documentation. The software also has powerful web applications at its disposal in order to integrate all employees and to support them effectively in the implementation of document-related processes.

Functions of the Document Management Software

  • Document Management & Control according to ISO
    Team or person-related processing and control of documents via team matrix with comprehensive rights concept
  • AI Assistant
    Creation of documents using the AI assistant
  • Version Management
    Access to historical document versions including change tracking and integrated PDF creation
  • Task & Escalation Management
    Overview of open tasks with automatic reminders via e-mail or intranet
  • Simple access for all employees
    Publication of documents via platform-independent WebCAQ.Net or export to MS Sharepoint®
  • Electronic Signature
    FDA 21 CFR Part 11 compliant
  • Applicable documents
    Add & view applicable documents easily
  • Variety of options for document processing
    Utilization of freely definable attributes with the option of displaying selected database content as active content in the documents
  • Import wizard
    Import existing documents easily using the wizard
  • All in one database
    Central storage of all documents in the CAQ database with access to master data (employees, cost units, customers, articles, suppliers, etc.)
  • Filter & search functions
    Simple access to relevant documents via filter function, full text search and keywords
  • Connection to document exchange portal
    Exchange documents with suppliers and customers easily via the qxhub portal

Cross-Modular Functions

Standards-Compliance of the Document Management Software

  • DIN EN ISO 9001 (e.g. Chapter 7.5)
  • IATF 16949
  • DIN EN ISO 13485
  • DIN EN 9100
  • DIN EN ISO/IEC 17025
  • FDA 21 CFR Part 820.40
  • FDA 21 CFR Part 11
  • GMP
  • IFS
  • More Regulations »
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