Veeva Vault Safety
Global End-to-End Adverse
Adverse event intake, processing, submissions,
and oversight with one global modern solution.
Veeva Vault Safety is a modern individual case safety report (ICSR) management system that supports intake, processing, and submission of adverse events for clinical and post-marketed products.
Within one system, sponsors and CROs process global and domestic adverse events for drug, biologic, vaccine, device, and combination products. Built-in gateway connections and reporting rules streamline submission management of cases to health authorities and distribution to partners.
Central coding dictionary management automates semi-annual MedDRA, WHODrug, and EDQM updates.
Why Vault Safety
Streamline adverse event management
Automate intake through submissionsGain ICSR process efficiencies from intake through case processing and submissions.
Seamless end-to-end safety processesSeamless process and data sharing between safety and clinical, quality, and regulatory applications with Vault Connections.
Global case view and oversightSee and process all global and domestic adverse events / cases and get oversight with real-time reports and dashboards.
Always stay currentSupport new regulatory requirements and access product innovation with 3 releases a year.