This resource is no longer available

The FDA's updated cybersecurity rules under Section 524B of the FD&C Act bolster medical device security to safeguard patient health and privacy. This white paper outlines the essentials:

• Definition of "cyber devices" and required premarket information from manufacturers
• Mandatory cybersecurity strategies, including vulnerability monitoring, patching, and coordinated disclosure
• Use of the NIST Cybersecurity Framework for robust device security

These FDA measures and guidance for manufacturers are crucial for countering threats to connected medical technologies. The full white paper details navigating Section 524B to ensure your devices are secure by design.

Vendor:

Wind River

Posted:

Jun 17, 2024

Published:

Jun 17, 2024

Format:

PDF

Type:

White Paper