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Business · 28/12/2016Updated: 10/17/2026 · 1 min read

FDA Releases Guidance on Managing Cybersecurity in Medical Devices

Summary

The Food and Drug Administration (FDA) has made available a new guidance document titled 'Postmarket Management of Cybersecurity in Medical Devices,' which outlines the agency's recommendations for managing postmarket cybersecurity vulnerabilities in marketed medical devices, and emphasizes the importance of manufacturers monitoring and addressing these vulnerabilities.

Original source language: Federal Register — Food and Drug AdministrationOpen original release →

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