Deep dives on FDA expectations, threat modeling, penetration testing, SDLC, and the standards your team is being asked to meet.
Showing 12 of 292 articles · Page 24 of 25
This guide emphasizes securing communication protocols in medical devices and provides actionable insights for manufacturers to enhance safety and privacy.
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How medJacking & MedHacking target medical devices, real-world examples, and the controls FDA expects manufacturers to implement in 2026.
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Step-by-step guide for medical device manufacturers to run a cybersecurity audit: scope, threat modeling, SBOM review, testing, and FDA-aligned documentation.
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In this post, we unravel this complex issue of cyber threats in medical devices and discuss what manufacturers can do to make their devices more secure.
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Securing Medical Devices for medical devices: step-by-step practices, FDA-aligned documentation, and pitfalls to avoid in 2026 submissions.
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Learn how ISO 14971 risk management applies to medical device cybersecurity - identify cyber hazards, control residual risk, and align with FDA. Aligned with.
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This article discusses the relationship between ISO 14971 and AAMI TIR57 / ANSI/AAMI SW96:2023, and how they help address risks in the production and use of medical devices.
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Updated July 24, 2026 Health Level 7 (HL7) is a vital cog in the machinery of healthcare information technology. Aligned with the FDA's Feb 3, 2026.
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This post covers the purposes, security risks, & regulatory guidance for medical device protocols for manufacturers, healthcare providers, & regulatory.
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The 10 ways cybercriminals monetize medical device breaches - and how MedTech teams can protect patient data, device safety, and clinical operations.
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SBOM + SAST explained: how component transparency and static code scanning strengthen medical device cybersecurity and align with FDA guidance.
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The 50 most common cybersecurity issues in medical devices, why each matters for patient safety, and how penetration testing catches them pre-submission.
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