Training: Usability, UX & risk management for medical devices

Why join this training?

This two-hour training is designed for designers, UX experts, Product Owners, and Functional Analysts working in the medical device field.

The training is given by Giliam Ganzevles, a leading expert in usability and UX for medical devices, with extensive experience in both academia and industry.

This is a rare opportunity to learn from an expert who combines deep academic knowledge with hands-on industry experience.

Usability directly impacts patient safety and regulatory compliance, and IEC 62366 defines how risk management and human factors engineering should be applied in medical device design.

Whether you're developing a new medical device or improving an existing one, this training will help you integrate usability and risk management into your design process the right way.

Please note that spots are limited to ensure a qualitative training. Save yours now!

What you will learn

Through clear explanations, real-world examples, and a practical approach, you will:

✅ Gain a clear understanding of IEC 62366 and its usability engineering framework.
✅ Learn how usability impacts risk management and patient safety.
✅ Discover strategies to design medical devices that are intuitive, safe, and compliant.
✅ Participate in an interactive Q&A session—get expert insights on your specific challenges.

This training is perfect for companies looking to refine their UX approach and ensure compliance while enhancing user experience.

Who Should Attend?

This training is ideal for:

1. Designers & UX Experts improving user interactions with medical devices.
2. Product Owners & Functional Analysts ensuring usability and regulatory alignment.
3. Regulatory & Quality Professionals who want to understand how usability affects compliance.

About Giliam Ganzevles

Giliam Ganzevles is a leading expert in usability and UX for medical devices, with extensive experience bridging academia and industry.

At HoGent HoWest, he teaches UX and usability principles.

He is also active as a senior consultant at Sunbird Medical Devices, where he helps companies integrate usability and risk management into their development processes.

Specializing in IEC 62366 compliance, human factors engineering, and patient-centered design, Giliam has worked with both startups and established MedTech companies to enhance usability while maintaining regulatory compliance.