Saturday, April 21, 2018

FDA's 'Medical Device Safety Action Plan' Focuses on Product Life Cycles and Preventing ...

The cybersecurity section of the plan details how the FDA will consider requiring companies to disclose to the agency and to medical-device customers a “Software Bill of Materials,” to keep them aware of devices that may be subject to vulnerabilities and speed up the postmarket mitigations process for ...

from Google Alert - vulnerability https://ift.tt/2HNRnnK
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