Deep-dive guides
Practitioner guides.
Long-form playbooks on medical device cybersecurity, FDA premarket submissions, and the leadership work behind high-performing technical teams. Written for people who have to ship.
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Deep-dive guide
Threat Modeling Connected Medical Devices: A Practitioner Guide
A threat model that survives FDA review names the asset, draws the trust boundary, enumerates every interface, classifies the threat, and ties each mitigation to a verifiable design control. Here is how to build one.
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Deep-dive guide
Postmarket Vulnerability Management for Connected Medical Devices
A workable postmarket cybersecurity program for connected medical devices: monitoring, triage, coordinated disclosure, patching, and the regulator-facing paper trail that proves it.
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Deep-dive guide
SBOM Hygiene for Medical Devices: A Practical 2026 Playbook
A working SBOM is not a file you generate once and ship. Here is how MedTech teams produce, maintain, and defend a Software Bill of Materials that survives FDA review and postmarket reality.
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Deep-dive guide
What the FDA Actually Wants in a 2026 Premarket Cybersecurity Submission
After 250+ FDA cybersecurity submissions cleared in 2025, here is what the FDA actually wants in your premarket package — and the seven mistakes that get you a Refuse-to-Accept.
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Deep-dive guide
Why Technical People Struggle With People Skills (And How to Fix It)
Technical people struggle with people skills because they're rewarded for being right, not for being understood. Here's the fix companies actually need.
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