"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:
Online Seminar
