Upcoming Training: IEC 62366 Medical Device Usability
This 1-day course on IEC 62366 Medical Device Usability, in collaboration with Intertek Academy, is designed to help professionals gain an understanding of the activities that should be implemented in a usability engineering process to fulfill the requirements of the MDR/IVDR.
📅 Next session: Online, 07 October 2026 (held in English)
🕘 Time: 09.00 – 16.00 CET
💰 Price: 8100 SEK/745 EUR (excluding tax)
Our upcoming IEC 62366 Medical Device Usability course, in cooperation with Intertek Academy, focuses on the usability engineering process, as described in the standard.
This course covers:
- History and regulatory context of the standard
- Usability – terminology and definitions
- The usability engineering process – step by step
- Formal usability validation
- Legacy devices
Who should attend?
Quality and regulatory professionals, user interface designers, or other professionals involved in key roles in medical device development.
What you’ll learn
You’ll walk away with a good understanding of what is required, from a regulatory perspective, to establish a usability engineering file for a medical device.
The course is led by Cilla Lundevall Wiberg, Medical Device QA/RA Expert.
Questions? Contact: academy@aurevia.com
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