Usability engineering according to IEC 62366-1
Usability engineering is an integral part of medical device development. It is important to understand how users may interact with a device, to avoid safety issues and to ensure its proper functioning.
To reduce the risk of use errors, both Medical Device Regulation (MDR) and In Vitro Diagnostic Medical Device Regulation (IVDR) require that devices are designed with respect to the intended use environment and the characteristics of the intended users. The IEC 62366-1:2015 +AMD1:2020 standard describes the various activities that should be implemented in a usability engineering process to fulfill the requirements of the MDR/IVDR.
This course focuses on the usability engineering process, as described in the standard. The course contains both theoretical sessions and practical exercises.
- When: to
- Where: Online
- Organizer: QAdvis in collaboration with Intertek
- Language: English
- Price: 7900 VAT not included