6th Human Factors & User Experience for Medical Device Design is a conference dedicated to Engineering Device Safety and Development through Usability Testing and Risk Mitigation
Topics
- Streamline strategies for risk management activities to improve overall device design
- Leverage usability testing early in the product development cycle to ensure a successful validation process
- Assess existing and forthcoming regulatory impacts to best meet compliance standards
- Establish internal alignment between design and human factors teams to improve product development
- Examine the European Medical Device Regulation (EU MDR) to provide clarity on transition timelines and expectations
Who should Attend
Attendees with responsibilities in:
- User Experience Design/ User Design
- Human Factors/Human Factors Engineer(ing)
- Industrial Design Design Controls/Engineer
- Usability/User Experience/User Interface/UX/UI
- Research & Development (R&D) Engineer
- Product Development
- Quality/Quality Control/Quality Assurance/Quality Engineer
- Device Engineering
- Regulatory Affairs
