In the evolving world of medical devices and combination products, understanding and applying Human Factors (HF) is not just a regulatory hurdle—it's a strategic key to commercial success. As regulatory expectations evolve and new technologies emerge across markets, how can you ensure your HF strategy is not only compliant but also a source of competitive advantage?
Join EPHMRA for a 45-minute webinar slot that moves beyond the basics to explore the application of HF research today, including 10-15 minutes for Q&A. We will ground the discussion in real-world case studies and highlight trends in the industry.
Speakers:
- Marissa Vallette, Vice President, User Experience and Human Factors, Ipsos
- Tom Snell, Associate Director, User Experience, Ipsos
Convenor:
- Michael Renz, Lead Medical Devices & Diagnostics Germany & Member EPHMRA Devices & Diagnostics Committee, Ipsos
Key Takeaways for Attendees
- Understand the strategic business case for HF beyond simple regulatory compliance.
- Gain practical insights from real-world case studies on how to integrate HF throughout the product lifecycle.
- Learn about emerging trends and innovative research methodologies.
- Appreciate the importance of global and cultural considerations in developing devices for diverse user groups.
Target Audience
This webinar is designed for professionals in the pharmaceutical, MedTech, and medical device industries, particularly those in roles related to Regulatory Affairs, R&D, Product Management, Marketing, and Device Engineering who are involved in the product development lifecycle.
UK time is quoted.
This is a member only event.