MedtecLIVE – 21st to 23rd of May 2019 in Nuremberg, Germany
CAQ AG will be presenting its sophisticated quality and product management solutions at the MedtecLIVE trade fair from the 21st to the 23rd of May 2019 in Nuremberg, Germany. Come visit us at stand 9-311 in hall 9 and find out more.
We have always been aware that the producers and suppliers of medical technology must adhere to the strict rules and regulations of the European Medical Device Regulation (MDR) and the US Food and Drug Administration (FDA). That is why we integrated and consistently maintain powerful functions and up-to-date guidelines in our software in order to assist you in all matters relating to quality management in the area of medical technology.
It therefore comes as no surprise that, for over thirty years, many medical technology companies have put their trust in the software solutions of CAQ AG Factory Systems in order to fulfil FDA-associated framework conditions and successfully master stringent quality management and validation processes.
Visit us at the MedtecLIVE in Nuremberg and find out how our software solutions can assist you in virtually all quality-related aspects of the medical technology sector.
Here are a couple of highlights:
- Supplier management in the medical technology sector with SRM.Net
- Standard-compliant CAPA workflow with sophisticated user guidance system
- Risk management in accordance with ISO 14971 including before/after risk matrix
- Fully scalable change control system with dynamic template management functions
- ISO 13485 compliant training management which links directly to your HR-system
- Comprehensive document management in accordance with the requirements of the FDA
- and much more