FDA Issues Draft Cybersecurity Guidance for Med Devices
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.
Author
Cynthia J. Larose
Member / 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.