"Do you want to collect requirements quickly and systematically 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? You just ask? Do a workshop? No! Henry Ford already knew: "If I had asked my customers what they wanted, they would have said a faster horse."
goalsThe making of requirements is not a matter of direct inquiry, chance or personal skill. Therefore, you will learn the following in the seminar:
- Process for collecting usage and system requirements
- Specification of user interfaces (user interfaces)
- Procedure for verification and validation of usability
- 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 , costs and registration . Unless otherwise noted in the table on the overview page, there are still vacancies.
KONTAKT:
Online Seminar