To reduce the risk of use errors, the Medical Device Regulation (MDR) requires that medical devices be designed with specific focus on the characteristics of the intended users. The IEC 62366-1 standard describes the various activities that should be implemented in a usability engineering process to fulfill the requirements of the MDR.
Information
When: Tue, 27 Sep 2022 08:30
to 15:30
Where: ONLINE
Organizer:
QAdvis AB
Language: English
Price:
6600
SEK
VAT excluded
Contact information
QAdvis AB
academy@qadvis.com
https://www.qadvis.com/portfolio-item/usability-engineering-according-to-iec-62366-1/