Live Webinar: Medical Device Cyber Testing
November 14, 1 pm EST. Register now!
Threat Modeling and Risk Assessment: A Step-by-Step Example
On-Demand Webinar - download now!
Why You Need a Secure Product Development Framework for Medical Device Cybersecurity
A Secure Product Development Framework is highlighted as a way of meeting QS regulations and FDA expectations.
Secure-by-Design: Using Hardware and Software Protection for FDA Compliance
Live Webinar, June 20 at 1 pm EDT!
Live Webinar: A Deep Dive into Secure Product Development Frameworks (SPDF)
May 16, 1 pm EDT. Register now!
A Deep Dive into Secure Product Development Frameworks (SPDF)
In our second webinar in our series of Cybersecurity In Medical Devices: Practical Advice for FDA’s 510(k) Requirements, we tackle the question of what is a SPDF for medical device cybersecurity. As with all webinars in this series we look to provide actionable advice that clarifies implementation, and you can apply in your day-to-day tasks.
8 SBOM Best Practices for Medical Device Manufacturers
A proactive approach to SBOM creation by medical device makers will contribute to a safer and more resilient healthcare ecosystem.
The Real-World Challenges of Medical Device Cybersecurity: Mitigating Vulnerabilities
Live Webinar, April 25. Register now!
The Real-World Challenges of Medical Device Cybersecurity: Mitigating Vulnerabilities
A great deal of attention in medical devices has shifted towards cybersecurity with the ratification of section 524B of the FD&C act. This new law enables the FDA to enforce cybersecurity controls in any medical device that is capable of networked communications or that has software. In this webinar we will recap the process for managing vulnerabilities, identify categories of vulnerabilities and solutions and more.
