Wednesday, February 5 • 11:15 AM - 12:00 PM Pacific Time (US & Canada); Tijuana
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Location: 202AB
Title: How to Avoid Engineering Your Product Twice: Mastering the New Cybersecurity Requirements for 510(k) Submissions
Description:
In this talk, we will guide you through the ever-evolving FDA cybersecurity regulations for 510(k) medical device submissions. Attendees who are experts will gain an up-to-date understanding of the latest requirements and best practices. Those who are new will gain a solid understanding of the basics. Key topics include threat modeling, secure product development frameworks, and the essential role of the Software Bill of Materials (SBOM). Learn practical strategies to ensure your device meets regulatory standards while maintaining development efficiency. Join us to gain the insights and tools needed to navigate these requirements and keep your development process on track.
Type: Design.Engineer.Build Conference
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