As Us Anything: Human Factors & Usability for Medical Device Development
As Us Anything: Human Factors & Usability for Medical Device Development
Date:
May 7, 2025
Presenters:
Denise Forkey & Jenny Collinson
Overview
Our inaugural thought leadership webinar featured an interactive Q&A session with our human factors experts addressing key challenges in medical device development. The session highlighted ClariMed's expertise in global regulatory strategies and practical implementation of human factors engineering processes.
Key Topics Covered
Global regulatory requirements for human factors validation across US, European, Chinese, and Japanese markets
Best practices for selecting appropriate user groups for human factors 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
Overview
Our inaugural thought leadership webinar featured an interactive Q&A session with our human factors experts addressing key challenges in medical device development. The session highlighted ClariMed's expertise in global regulatory strategies and practical implementation of human factors engineering processes.
Key Topics Covered
Global regulatory requirements for human factors validation across US, European, Chinese, and Japanese markets
Best practices for selecting appropriate user groups for human factors 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
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