What is required, from a regulatory perspective, to ensure good usability for a medical device.
This event has expired
This course focuses on the usability engineering process, as described in the standard. The course contains both theoretical sessions and practical exercises.
Topics
- History and regulatory context of the standard
- Usability – terminology and definitions
- The usability engineering process – step by step
- Formal usability validation
- Legacy devices
Information
- When: to
- Where: Online
- Organizer: QAdvis in collaboration with Intertek Academy.
- Language: English
- Price: 7900 VAT not included
Registration
Please register no later than Tuesday 7 January 2025
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