• Independent testing of medical devices, in particular with regard to:
    Aspects of ergonomic design, usability and human errors (e.g. within the scope of medical device approval)
  • Consulting and training of developers, manufacturers and users (inter alia normative approval requirements and practical procedures for ensuring and evaluating ergonomic quality and usability as well as HMI safety)
  • Research on new approaches, methods and tools in the field of ergonomic design, usability evaluation and optimization of medical devices and systems
  • Support for developers and manufacturers regarding questions of ergonomic design, usability and human risk analysis
  • Support for users (e.g. clinics) in the evaluation / comparison of the usability of medical devices in the context of procurement measures as well as within the integration into medical application processes