Usability engineering according to IEC 62366-1
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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: to
- Where: ONLINE
- Organizer: QAdvis AB
- Language: English
- Price: 6600 VAT not included
Registration
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"startDate":"2022-09-27",
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"endDate":"2022-09-27",
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