"Want to collect requirements quickly and automatically and create a lean, IEC-62366-compliant usability file?"

How do you find out what requirements your customers and users have of a medical device? Should you just ask? Do a workshop? No! Henry Ford had the right answer: "If I had asked my customers what they wanted, they would have said a faster horse."

aims

The making of requirements is not a matter of direct inquiry, chance or personal skill. You will learn the following in this seminar:

  • The process for collecting usage and system requirements
  • Specification of user interfaces (user interfaces)
  • The procedure for verification and validation of usability
  • The development process compliant with IEC 62366-1 and IEC 60601-1-6 and the interaction with ISO 14971
  • Legally compliant usability file ("Usability File")

Here you will find further information on the next dates and costs. Unless otherwise noted in the table on the overview page, there are still free spots available.

KONTAKT:
Konstanz - Rheingarten

 

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