Every article in our archive in Fundamentals.
Looking for a quick answer instead? The FDA medical device cybersecurity FAQ covers Section 524B scope, SBOMs, threat models, CR515 and GMLP, deficiencies, and postmarket duties.
Showing 12 of 44 articles in Fundamentals · Page 1 of 4
What is MedTech, and how does it differ from a medical device or life sciences? Clear definitions, from scalpels and sutures to connected cyber devices.
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How CVSS scoring works for medical devices, a worked scoring example, and why a raw score is not a patient risk score under FDA guidance.
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Medical device software development explained: design controls, IEC 62304 safety classes, SOUP management, verification, validation, and FDA documentation.
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You're two years into product development and still "not ready" for cybersecurity? You're already late.
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Why CVSS 4.0's Safety and Automatable metrics matter for patient harm, and how to handle the transition in FDA submissions and postmarket VEX statements.
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Understand whether to hire a medical device security consultant or build an in-house team. Evaluate costs, FDA expertise, and submission timelines.
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Medical device cybersecurity fundamentally differs from enterprise IT due to patient safety, FDA regulations, and unique technical constraints. Learn why.
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How to choose a medical device cybersecurity company: 5 criteria that set FDA specialists apart from generalists, plus questions that reveal real depth.
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Postmarket device cybersecurity is a shared job. See how manufacturers and healthcare organizations collaborate to reduce risk once a device is deployed.
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Learn the difference between SaMD and SiMD, why it matters for FDA strategy, and how to build secure-by-design medical devices across your product.
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Discover the truth behind the top 5 medical device cybersecurity myths and how debunking them drives innovation, safety, and FDA compliance today.
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Discover how MedTech innovators use cybersecurity as a strategic advantage to gain investor trust, meet FDA expectations, and drive market success.
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