Deep dives on FDA expectations, threat modeling, penetration testing, SDLC, and the standards your team is being asked to meet.
Showing 12 of 360 articles · Page 25 of 30
Learn how attackers abuse PowerShell in MedTech environments - and how to harden endpoints, logging, and admin access to support FDA-ready cybersecurity evidence.
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Learn OWASP-aligned file upload validation techniques - type checks, storage isolation, malware scanning, and testing - tailored for regulated environments.
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Manage local admin passwords on Windows-based medical devices safely. Why GPP is risky, and how Windows LAPS supports rotation, control, and audits.
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Learn what return-to-libc attacks mean for medical device cybersecurity - and how to reduce risk with memory protections, secure coding, and testing.
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Safer alternatives to Tor for MedTech teams: dark web monitoring, breach intel, and postmarket-ready workflows to reduce risk in IoMT ecosystems.
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Biometrics improve usability - but can be spoofed. Learn “gummy finger” risks, liveness/PAD, and FDA-ready controls for medical device ecosystems.
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Discover how cybersecurity failures in medical devices have led to recalls and potential risks for patients.
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Learn how device cloning threatens medical device security and how manufacturers can defend against spoofing risks to meet FDA cybersecurity expectations.
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Bluetooth Low Energy is core to CGMs, pacemakers, and wearables. Common BLE attack vectors and the controls FDA expects in premarket submissions.
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Cyber attribution is uncertain by design. Learn why, what evidence holds up, and how MedTech teams should respond for FDA-aligned risk management.
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Learn how birthday attacks exploit hash collision probability - and what MedTech teams should do (SHA-256+, signing, truncation rules, testing, evidence).
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Use GHDB as a defensive OSINT check to find unintended public exposure in medical device ecosystems - cloud portals, docs, and support sites - and fix it fast.
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