As Us Anything: Human Factors & Usability for Medical Device Development

ClariMed's inaugural thought leadership webinar brought human factors experts together for an open Q&A on the practical challenges of medical device development. The session addressed global regulatory requirements, study design, and how to embed human factors engineering across the full product lifecycle from early development through market entry.

Key Topics Covered:

• Global regulatory requirements for human factors validation across the US, EU, China, and Japan

• Best practices for selecting appropriate user groups for validation testing

• Strategies for integrating human factors engineering throughout the product development lifecycle

• Balancing innovation with safety and regulatory compliance

• Current trends in medical device usability and their impact on development processes