Veeva Safety
Global End-to-End Adverse
Event Management
Adverse event intake, processing, submissions,
and oversight with one global modern solution.
Announced 2019 Status Mature Customers 51-100
Hear how Merck streamlines processes with unified safety
Overview
Global oversight and streamline case management, submission, distribution
Veeva Safety is a modern individual case safety report (ICSR) management system that manages 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.
Hear from biopharmas transforming pharmacovigilance with Veeva Safety.
Why Veeva Safety
Streamline adverse event management
Customer Success
Improve safety oversight and case processing
with one global solution
Resources
Explore and Learn
Watch video
Streamline package insert management: Veeva Safety to Veeva RIM
Read blog post
Improve oversight and data control when outsourcing
Read blog post
Building a safety intelligence unit from the ground up
Hear how
Transform pharmacovigilance with Veeva Safety
Watch demo series
See the latest capabilities and best practices in Veeva Safety
Read case study
Better control of and access to the safety data
