"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 for a medical device? you just ask? Conduct 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)
- Procedures 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. If nothing else is noted in the table on the overview page, there are still places available.
KONTAKT:
Konstanz - Rheingarten
