Date: April 22, 2025
Time: 2:00 PM ET
Registration Link: Register Now
Medical device security is rapidly evolving, and with the FDA’s latest cybersecurity regulations in effect, manufacturers must be proactive in identifying and mitigating software vulnerabilities.
However, securing Class II and Class III medical devices is a complex challenge that impacts patient safety, compliance, and operational efficiency.
On April 22, 2025, at 2:00 PM ET, join Health-ISAC and Shane Fry, CTO of RunSafe Security, for a live discussion on navigating postmarket cybersecurity challenges. Learn how to efficiently identify vulnerabilities, streamline patching processes, and comply with FDA postmarket cybersecurity requirements.
Key Takeaways:
- Identifying Vulnerabilities: How to use Software Bill of Materials (SBOMs) to uncover risks in medical device software.
- Patching & Postmarket Security: Strategies for mitigating high-risk vulnerabilities and supporting compliance with FDA cybersecurity regulations.
- Real-World Case Study: How a medical device manufacturer discovered and addressed over 2,000 vulnerabilities, including high-severity memory safety issues.
Don’t miss this opportunity to enhance your approach to medical device security and compliance.
Register now to secure your spot!
Meet Our Speakers:
Shane Fry, CTO, RunSafe Security
Meet Our Moderator:
Moderator: Health-ISAC
