Practical Guide to Cybersecurity and SBOM Management for FDA Approval

As medical devices become increasingly cloud connected, ensuring their security is more important than ever. This webinar dives into four key areas:

• Threat Modeling

• Risk Assessment

• SBOM Management

• Post-Market Monitoring for Cybersecurity.

  Key Takeaways:

1. Threat Modeling for Medical Devices: Learn how to identify and address security threats specific to medical device software during the design and development phases to ensure patient safety.

2. Risk Assessment in Healthcare Devices: Understand how to assess cybersecurity risks in medical devices, including compliance with FDA, IEC 62304, and other industry standards.

3. SBOM Management for Medical Devices: Gain strategies for managing Software Bills of Materials (SBOM) to improve supply chain visibility and mitigate vulnerabilities in third-party software components.

4. Post-Market Cybersecurity Monitoring: Discover how to establish a continuous monitoring plan for medical devices once they are in use, ensuring you can respond to emerging threats and maintain compliance with regulatory requirements.

Webinar by Darcy Bachert, CEO and founder Prolucid Technologies.