Veeva Safety

Global Adverse Event Management and Oversight

Safety is a modern individual case safety report (ICSR) management system that manages the intake, processing, and submission of adverse events for clinical and post-marketed products.

Within one system, sponsors and CROs process and manage global and domestic adverse events for drug, biologic, vaccine, device, and combination products. Built-in gateway connections and reporting rules streamline submissions to health authorities and distributions to partners.

Central coding dictionary management automates semi-annual MedDRA, WHODrug, and EDQM updates.

Hear from biopharmas transforming pharmacovigilance with Veeva Safety.

Announced 2019 Status Mature Customers 51-100
Veeva Safety | Modern Adverse Event & Case Management System
Hear how Merck streamlines processes with unified safety
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Overview

Global Adverse Event Management and Oversight

Safety is a modern individual case safety report (ICSR) management system that manages the intake, processing, and submission of adverse events for clinical and post-marketed products.

Within one system, sponsors and CROs process and manage global and domestic adverse events for drug, biologic, vaccine, device, and combination products. Built-in gateway connections and reporting rules streamline submissions to health authorities and distributions to partners.

Central coding dictionary management automates semi-annual MedDRA, WHODrug, and EDQM updates.

Hear from biopharmas transforming pharmacovigilance with Veeva Safety.

Veeva AI for Safety
See in Action
Veeva Falcon

Standard AI agents that do the work for you. Automate safety intake and triage for faster, more efficient case processing.

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Vault AI

Enhance case narratives by correcting grammar, consolidating information, and improving readability.

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Why Veeva Safety

Streamline adverse event management

Customer Success

Improve safety oversight and case processing
with one global solution

CRISPR UCB LEO Merck