FREE LIVE WEBINAR

April 15th | 12 PM to 1:00 PM ET

Use related risk analysis & how it applies to medical device development

As the landscape of medical device regulations continues to evolve, it’s crucial to stay ahead of the curve when it comes to Use-Related Risk Analysis (URRA). This webinar is designed to equip professionals with the knowledge needed to identify, assess, and mitigate use-related risks effectively.

What You Will Learn:
  • URRA Fundamentals: Understand the core concepts and why URRA is essential for medical device safety.

  • Integrating HFE: Learn how URRA works in tandem with Human Factors Engineering (HFE) to enhance user safety.

  • Regulatory Insights: Get up-to-date guidance on FDA expectations for URRA compliance.

  • Practical Strategies: Discover proven methods for identifying and mitigating use-related risks.

  • Case Studies: See real-world examples of URRA in action to understand its practical application.

Register for the Live Webinar

Gilero Webinar
Who should attend?
  • Quality Professionals and Management
  • Regulatory Affairs Professionals & Management
  • Medical Device Executives
  • Product Development Engineers and Management
  • Risk Managers
  • Clinical Professionals and Management
Register Now  

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