Medical Device Cybersecurity Resources

How to Systematically Identify Cybersecurity Threats and Meet FDA Requirements Summary STRIDE for medical devices provides a systematic approach to identifying cybersecurity threats throughout the device development lifecycle. This comprehensive framework helps quality, regulatory, and engineering teams categorize threats into…

Cybersecurity Traceability Matrices FDA Will Expect to See in Your Medical Device Submission Summary In this article, you’ll learn: Introduction A cybersecurity traceability matrix is more than just documentation—it’s your roadmap showing FDA how you’ve systematically addressed security risks throughout…

Your Medical Device is Cleared. Your Security Job Just Started. Summary Introduction: The Post-Market Reality Check Your medical device just received FDA clearance. The champagne bottles are empty, the team is celebrating, and you’re ready to move on to the…

FDA Updates Cybersecurity Guidance: Key Changes and Clarifications The FDA released an updated version of its cybersecurity guidance document for pre-market submissions on June 27, 2025, marking the first revision since the original September 2023 release. Below you’ll find redlined…

How FDA’s Secure Product Development Framework Enhances Software Lifecycle Processes While Requiring Separate Documentation Packages TL;DR Understanding SPDF vs IEC 62304 is crucial for medical device teams navigating today’s regulatory landscape. SPDF (Secure Product Development Framework) is “a set of…

Failure to build your medical device on a secure architecture costs millions and puts patients at risk Poor security architecture choices early in device design create problems that last for years. When companies try to add security features after they…

Explore the innovative application of the Common Vulnerability Scoring System (CVSS) in medical device risk assessment.

Discover essential strategies for safeguarding your digital assets with our comprehensive guide on implementing cybersecurity controls.

Discover the essential steps and best practices for conducting effective penetration testing.

Discover the essential steps to integrate security into every phase of your software development lifecycle.

Discover the essential steps and best practices for conducting a thorough security code review.

Unlock the secrets of creating effective data flow diagrams tailored for medical devices.

Learn how to develop a robust architecture security view for your medical device, aligning with FDA cybersecurity guidelines, AAMI TIR57, AAMI SW96, and industry best practices. Introduction As medical devices become increasingly interconnected, cybersecurity threats pose a significant risk to…

Learn how to create an effective patch management and security update process to protect your systems from vulnerabilities. This guide covers best practices, tools, and strategies to ensure your software and hardware are always up-to-date and secure.

Learn how to perform threat modeling for cloud-connected medical devices leveraging FDA’s 2023 cybersecurity guidance and standards such as AAMI TIR57 and AAMI SW96. Introduction With the rise of connected healthcare, medical devices increasingly integrate embedded systems, mobile applications, and…