Cybersecurity & Penetration Testing for Medical Devices

On-demand Webinar

Learn how to protect medical devices from cyber threats and meet U.S. FDA requirements with effective testing. 

With cybersecurity now a regulatory requirement – not just a best practice – medical device manufacturers must prove their products are secure. Join TÜV SÜD’s upcoming webinar to learn how penetration testing supports compliance with the U.S. FDA’s medical device cybersecurity requirements, validates device safety, and helps you act on test results with confidence. Whether you're preparing a premarket submission or strengthening your security posture, this session may give you the clarity and tools to move forward. 

Key Takeaways:

• Learn what the FDA expects for medical device cybersecurity testing. 
• Understand how penetration testing validates real-world device safety. 
• Know how to act on test results in a way that satisfies FDA requirements. 
  
  

Exclusive Offer for Attendees – Free Attack Vector Analysis

All webinar participants will have the opportunity to request a complimentary Attack Vector Analysis of their medical device. This analysis – a valuable first step toward penetration testing, often recommended by the FDA – helps identify potential cybersecurity vulnerabilities in your device. By taking advantage of this free offer, you can engage your development team early, gain objective insights into your device’s security posture, and ensure you’re aligning with FDA expectations before embarking on a full penetration test. (Details on how to request the free analysis will be provided during the webinar.) 

Speakers 

Grace Lee
Cybersecurity Engineer & Penetration Tester, TÜV SÜD MHS Korea 
Grace Lee is a cybersecurity engineer and certified penetration tester at TÜV SÜD Medical Health Services in Korea. She holds OSCP, OSWP, and CRTO credentials and has extensive experience helping medical device manufacturers meet FDA and MDR cybersecurity requirements. 

Edoardo Pozzi
Europe Testing Sales Manager, TÜV SÜD Medical Health Services 
Edoardo Pozzi is the Europe Testing Sales Manager at TÜV SÜD MHS. He has broad experience in medical device testing and compliance. Edoardo will moderate the webinar and lead the 15-minute Q&A, bringing audience questions to the expert. 

Register now to secure your spot for this informative webinar on Feb 26 and get practical guidance on keeping your medical devices secure and FDA-compliant.