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We all know: ensuring the safety and efficacy of medical devices is critical to protecting patients and minimizing risks to healthcare providers.
One of the key challenges in achieving this goal is selecting and managing materials effectively, while maintaining supplier controls and identifying opportunities for proactive design changes.
In this panel discussion, experts in medical device development, regulatory compliance, and material science will share their insights on navigating material risks and implementing strategies to improve medical device safety.
Topics will include:
Attendees will come away from this session with a better understanding of how to navigate material risks in medical device development and implement effective strategies for improving safety and quality.
Please register now to reserve your spot and ask our team questions live!