Discover the changing terrain of medical device cybersecurity regulations, and gain invaluable insights from our panel of experts. Join us for an in-depth exploration of "Navigating the New FDA Cyber Device Landscape." Our team of experts will walk you through the fundamental aspects of the updated FDA cyber device criteria and its profound impact on your software/system development protocols and the lifecycle of maintenance.
Embark on a journey through the entire product development and risk management lifecycle. Uncover the critical elements of pre-market and post-market cybersecurity risk management, encompassing areas such as threat modeling, the creation and maintenance of software bill of materials (SBOM), vulnerability assessments, effective strategies for coordinated vulnerability disclosure, and the development of practices to preempt the regulatory pitfalls.