This poster provides a comprehensive overview of governance, risk management, and compliance in medical device cybersecurity, highlighting both the evolving regulatory landscape and Velentium Medical’s structured approach to secure product development.

Attendees will gain insight into how global regulatory expectations — including FDA cybersecurity guidance, IEC 81001-5-1, ANSI/AAMI SW96, and other international standards — shape the requirements for secure design, risk assessment, labeling, testing, and postmarket activities. The center of the poster features Velentium Medical's end-to-end medical device cybersecurity process, which integrates cybersecurity across the Total Product Lifecycle, from initial requirements and architecture through end of support.

This session is intended for professionals responsible for product security strategy, regulatory submissions, and lifecycle risk management, offering a clear visual framework and actionable insights into aligning cybersecurity practices with industry-leading standards and expectations.