Veeva Vault Safety

Global End-to-End Adverse
Event Management

Adverse event intake, processing, submissions,
and oversight with one global modern solution.

Announced 2019
Status EARLY
Customers 51-100

Veeva Vault Safety is a modern safety case management system that manages intake, processing, and submission of adverse events for clinical and 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 for case submissions and tracking 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

  • Improve pharmacovigilance oversight

    Real-time reports and dashboards with seamless partner collaboration for risk mitigation and compliance.
  • Streamline intake to submissions

    Gain efficiency and automate the end-to-end intake, case processing, and submission process.
  • Global view of adverse events & cases

    See all global and domestic adverse events or cases for drug, biologic, device, and combination products.
  • Always stay current

    Support new regulatory requirements or access recent capabilities with automatic upgrades.


Explore and learn

Streamline package insert management: Vault Safety to Vault RIM
Watch video
Connect safety data across value chain to improve patient safety
Read article
Better control of and access to the safety data
Read case study

Interested in learning more about how Veeva can help?