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Medical device cybersecurity is no longer optional—it’s a regulatory and operational imperative. This webinar, hosted by Blue Goat Cyber and featuring cybersecurity leaders Trevor Slattery and Jordan John, delivers a deep dive into the five most essential standards and guidance documents shaping the cybersecurity landscape for medical devices. From AAMI TIR57 to NIST 800-115, FDA premarket guidance, ISO/IEC 81001-5-1, and IEC 62304, we’ll break down what each document covers, why it matters, and how to apply them strategically in your device development and submission process. What You’ll Learn: The role of each standard in securing medical devices How these documents tie into FDA expectations for 510(k), De Novo, and PMA submissions Practical tips for integrating cybersecurity into your QMS and design controls Insights into postmarket compliance and vulnerability management Whether you're a regulatory affairs professional, a device developer, or a security lead, this session will give you actionable knowledge to meet compliance with confidence. 🎙️ New to streaming or looking to level up? Check out StreamYard and get $10 discount! 😍 https://streamyard.com/pal/d/50868392...