Our foundation is built on over many years of heritage expertise.
Provide an intuitive and engaging reporting experience that works on users’ preferred devices and in their local language.
Achieve global consistency with a single, centralized, and fully audit-trailed solution for all intake routes and follow up.
Streamline pharmacovigilance processes by digitizing intake, output, and eliminating manual steps.
Unified capture of data through a single workflow engine enabling digital intake at source or automatic import of structured forms across languages.
Tailored experience based on user type, product, and nature of adverse events.
Eliminate manual reconciliation through automated E2BR2/R3 transfer into the safety database.
High availability and high-performance cloud infrastructure to manage rapid shifts in adverse event reporting.