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)
May 16, 1 pm EDT - 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.
Cybersecurity in Medical Devices – Practical Advice for FDA’s 510(k) Requirements
Live Webinar, March 12. Register now!
Cybersecurity in Medical Devices – Practical Advice for FDA’s 510(k) Requirements
Don’t miss this important webinar with partners BG Networks and Trustonic, which serves as a roadmap for medical device manufacturers to navigate the complex landscape of FDA requirements and implement effective cybersecurity measures.
SaMD vs. SiMD: Do You Know the Difference?
Though the terms SaMD and SiMD are often used interchangeably, understanding their nuances is crucial for navigating compliance.
