The document provides an overview of Veeva's approach to simplifying postmarket surveillance for medical devices. It discusses the challenges companies face with current postmarket surveillance programs, including systems that have become too complex and difficult to use over time. Veeva proposes a unified, connected solution on their Vault platform called Vault Product Surveillance, which would provide standardized adverse event reporting, a global complaint decision tree, and integration with other Vault quality applications. This is aimed at improving user experience, standardizing best practices, and accelerating implementation compared to customizing separate systems. The presentation also outlines how Veeva's approach could help organizations modernize their postmarket surveillance.