• Version
• Download 76
• File Size 0.00 KB
• File Count 1
• Create Date August 1, 2025
• Last Updated August 1, 2025

Key Takeaways and Best Practices of China Human Factor/Usability

Join us for an in-depth webinar on the fundamentals of human factor/usability, with a special focus on the unique aspects and standards in China. Starting from October 8, 2024, usability engineering documents need to be submitted for medical device applications in accordance with the new guideline, “Registration Review Guideline for Medical Device Usability Engineering (2024, NO.13)”, published in Mar 2024. Since then, we have successfully assisted our clients in submitting human factors documentation and have received the first batch of feedback from the NMPA. In this session, we would like to take this opportunity to share our experiences and insights and enhance the knowledge of usability principles and practices.

Agenda:
1. Usability Fundamentals
Usability Regulations and Standards
Introduction to China's Usability Engineering Guidelines: Gain insights into the principles guiding usability engineering in China, including the latest guidelines published in 2024.

2. Usability Testing
Planning Usability Testing : Learn how to design comprehensive usability testiing plans.

Executing Usability Testing: Discover best practices for conducting effective usability testing.

Analyzing Testing Data: Understand methods for analyzing usability testing data to extract meaningful insights.

Case Studies and Discussions: Participate in case study analyses and discussions to apply usability testing concepts in real-world scenarios.
This webinar will provide you with the knowledge and tools needed to navigate the evolving landscape of usability engineering, particularly in the context of China's regulatory environment. Don't miss this opportunity to enhance your expertise and stay ahead in the field.

Attached Files