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Case Study

Let's Talk Risk! Podcast

Case Study: Why FDA Cybersecurity Expectations Are Really QMS Expectations

Published
July 10, 2026
Duration
17:29
Summary source
description
Last updated
Aug 19, 2026

Discusses You cannot bolt cybersecurity onto a medical device at the end of development.FDA’s cybersecurity gu…

Summary

You cannot bolt cybersecurity onto a medical device at the end of development.FDA’s cybersecurity guidance makes a clear shift: cyber risk is now a quality system issue, a patient safety issue, and a lifecycle management issue. For connected and software-enabled devices, it is not enough to show that the software works as intended. Manufacturers also need…

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Show notes

You cannot bolt cybersecurity onto a medical device at the end of development.FDA’s cybersecurity guidance makes a clear shift: cyber risk is now a quality system issue, a patient safety issue, and a lifecycle management issue. For connected and software-enabled devices, it is not enough to show that the software works as intended. Manufacturers also need to show how cybersecurity risks were identified, controlled, verified, traced to patient harm, and managed after release.In this audio summary