Keeping up-to-date with regulations
Swiss Medtech offers application-oriented educational programmes, together with SAQ-QUALICON and the TÜV SÜD Academy. The seminars provide medtech specialists with information on the latest regulatory developments - from the EU Medical Devices Regulation (MDR) to «ISO 13485:2016».

Image source: Swiss Medtech
Image source: Swiss Medtech

The TÜV SÜD Academy and SAQ-QUALICON offer furthering education courses covering regulatory requirements for market introduction and monitoring, as well as on documentation and traceability of products under the new EU MDR regulations (among others). This includes information regarding ISO standard 13485:2016, which helps companies optimise quality management over the entire product life cycle.

The one to several-day seminars and courses are mainly tailored to quality management and quality assurance specialists who are responsible for fulfilling the specific requirements for medical products.


Substatiated, modular, and practical
The furthering education courses are well-founded and designed in a practical, modular manner. The qualifications and certifications obtained meet the highest quality standards worldwide.

SAQ-QUALICON is a recognized educational and consulting organisation in Switzerland which focuses on Quality Assurance as well as Quality and Process Management. The TÜV SÜD Academy is one of the world's leading training partners in the areas of technology, management, and healthcare. The course programme is supported by the Economic Development Agency of the Canton of Solothurn.

Courses shqa-acedemy

  • Annual agenda of shqa (DE)
  • Members of Swiss Medtech receive a CHF 100.- per day discount on all offers.
  • Contact shqa: 041 500 07 80