Navigating FDA’s New Cyber Device Paradigm - Cybersecurity & Compliance, Industry Best Practices

The evolving landscape of medical device cybersecurity regulations calls for a comprehensive understanding of the new FDA cyber device paradigm. Join our exclusive webinar where experts will delve into the intricacies of compliance and cybersecurity, providing valuable insights into best practices for designing, developing, and maintaining cybersecure medical devices.

We’ll explore, "Best Practice Development for the New FDA Cyber Device Paradigm." Our experts will guide you through the essentials of the new FDA cyber device criteria and its impact on your software/system development procedures and maintenance lifecycle.

We’ll journey through the product development and risk management lifecycle and learn about pre and post market cybersecurity risk management including, threat modeling, creating, updating, and monitoring software bill of materials (SBOM), vulnerability assessments, effective coordinated vulnerability disclosure strategies, and developing practices to avoid the new gotcha elements within the regulation.

Don't miss this chance to enhance compliance, cybersecurity practices within your organization and bring more secure devices to market.