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.
When: Tue, 27 Sep 2022 08:30 to 15:30
Organizer: QAdvis AB
Price: 6600 SEK
Link to website or email address