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# Device Cybersecurity Clarifications in FDA Webinar
- URL: https://www.fdaweb.com/device-cybersecurity-clarifications-in-fda-webinar/
- Published: 2022-05-20T12:00:00.000Z
- Updated: 2026-09-14T17:45:23.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5151861

FDA has announced a [6/14 Webinar](https://www.fda.gov/medical-devices/workshops-conferences-medical-devices/webinar-cybersecurity-medical-devices-quality-system-considerations-and-content-premarket?utm%5Fsource=CDRHTwitterD) to share information and answer questions about its recent draft [guidance](https://www.fda.gov/regulatory-information/search-fda-guidance-documents/cybersecurity-medical-devices-quality-system-considerations-and-content-premarket-submissions?utm%5Fmedium=email&utm%5Fsource=govdelivery) entitled “Cybersecurity in Medical Devices: Quality System Considerations and Content of Premarket Submissions.” FDA [says](https://content.govdelivery.com/accounts/USFDA/bulletins/312356d?ref=fdaweb.com) the new version is intended to “further emphasize the importance of ensuring that devices are designed securely, enabling emerging cybersecurity risks to be mitigated throughout the total product lifecycle and to outline FDA’s recommendations more clearly for premarket submission content to address cybersecurity concerns.” The Webinar is intended to:

- Describe the differences between 2018 and 2022 drafts
- Describe the guidance’s general principles
- Describe the design and documentation recommendations