FDA Issues Draft Cybersecurity Guidance for Med Devices

By Cynthia J. Larose

If you are a medical device manufacturer, the Food and Drug Administration (FDA) says that you should prepare a “cybersecurity bill of materials” before marketing your devices.  As outlined in our sister blog’s post, the requirement would require manufacturers to produce a list of the components that could be susceptible to vulnerabilities.   Read on here.

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  • Privacy & Cybersecurity

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  • Cynthia J. Larose
  • Benjamin M. Zegarelli

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  • Privacy & Cybersecurity
  • FDA Regulatory

    • Author

    Cynthia J. Larose

    Member / Co-Chair, Privacy & Cybersecurity Practice

    Cynthia J. Larose is Chair of the firm's Privacy & Cybersecurity Practice, a Certified Information Privacy Professional-US (CIPP-US), and a Certified Information Privacy Professional-Europe (CIPP-E). She works with clients in various industries to develop comprehensive information security programs on the front end, and provides timely counsel when it becomes necessary to respond to a data breach.