Quartica’s MARS Platform is the leading AI solution for pharmacovigilance departments, covering every aspect of generating, managing, and planning PV activities for everything outside of ICSR processing. Unlike other solutions which focus on individual areas of a PV Department, MARS takes a holistic, platform approach to support and force multiply entire teams (and ROI). MARS can handle both local and global requirements, as well as generate documents for all types of products from pharmaceuticals to cosmeceuticals. Built with compliance at its core, MARS ensures that every document and process aligns with the latest regulatory standards, reducing risk and streamlining audits. Designed by industry experts who understand the day-to-day challenges of pharmacovigilance, the platform is packed with thoughtful features that enhance efficiency, accuracy, and collaboration. From automated workflows to intuitive reporting tools, MARS simplifies complex processes while maintaining the highest level of compliance, empowering PV teams to focus on what matters most—patient safety and operational excellence.