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.
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När: Tis, 27 sep 2022 08:30 till 15:30
Arrangör: QAdvis AB
Pris: 6600 SEK