Contact Person

Térésa Nüsse

Tel. +49 2339 9182-214

The quality management software for medical technology and the pharmaceutical industry

CASQ‑it is so successful in the medical technology and pharmaceutical industry because the required documentation and verification requirements are met with absolute reliability. This is achieved with a seamless and secure paper trail, continuous monitoring and evaluation of all actions taken and 100% traceability.

Compliance security with the CAQ Software CASQ-it

Geared precisely to the specific requirements of the medical and pharmaceutical industry, CASQ‑it provides transparency and security through an integrated rights concept with clear responsibilities, complete documentation of all production-related processes, traceability back to the individual inspection reading and centralized recording of all corrective, preventive and emergency measures. The entire range of CASQ‑it modules meets the requirements of rule-oriented software validation and supports processes in compliance with the ISO 9001, FDA and DIN EN ISO 13485 standards.


  • Continuous batch tracking.
  • Digital signature.
  • Quality documentation with individual, company-specific approval certificates.
  • Rigorous quality assurance with systematic error prevention strategies starting in the development phase.
  • Complaint and error tracking with built-in escalation management.
  • Management information system: company-wide quality management information system with drill-down analyses.
  • Comprehensive quality reports at the click of a mouse or fully automatically.
  • Adjustable warning systems: immediate notification when a preset limit is exceeded.


CASQ‑it supports your processes and complies with

  • ISO 9001
  • FDA
  • DIN EN ISO 13485.

Modules for the medical technology and pharmaceutical industry

All CASQ‑it modules which are successfully used in the medical technology and pharmaceutical industry can be found in the column on the left.