Human Factors Engineering: The Worldwide Guide for Medical Device Manufacturers

This on-demand webinar, hosted by Greenlight Guru, delves into the intricate process of human factors engineering in the medical device industry. With a focus on meeting regulatory requirements across major global markets like the United States, United Kingdom, and European Union, this webinar is essential for understanding the complexities of human factors engineering worldwide.
Main points covered:
1. Clarification of human factors engineering requirements.
2. Detailed overview of the human factors engineering process.
3. Adaptation of human factors efforts for different markets.
4. Documentation needed for human factors engineering submissions.
Target Audience:
• Medical Device Executives
• Regulatory Affairs Professionals
• R&D Professionals
• Quality Professionals
• Human Factors/User Experience (UX) Professionals
Access the printable slides for this presentation by visiting:
www.greenlight...