³Ô¹Ï±¬ÁÏ 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 ³Ô¹Ï±¬ÁÏ Safety.
Announced 2019 Status Mature Customers 51-100
Read how ³Ô¹Ï±¬ÁÏ Falcon Safety reduces costs and accelerates safety operations
Why ³Ô¹Ï±¬ÁÏ Safety
Streamline adverse event management
Customer Success
Improve safety oversight and case processing
with one global solution
Resources
Explore and Learn
Read Features Brief
³Ô¹Ï±¬ÁÏ Safety Features Brief
Read Press Release
³Ô¹Ï±¬ÁÏ Falcon Safety to Work with All E2B-Compliant Safety Systems
Watch Demo
Submitting ICSRs Using FDA E2B(R3) Standard
Learn More
Safety for Emerging to Growing Biotech and Biopharma
Watch Video
Streamline Package Insert Management: ³Ô¹Ï±¬ÁÏ Safety to ³Ô¹Ï±¬ÁÏ RIM
Read Blog Post
Building a Safety Intelligence Unit from the Ground Up
Hear How
Transform Pharmacovigilance with ³Ô¹Ï±¬ÁÏ Safety
Watch Demo Series
See the Latest Capabilities and Best Practices in ³Ô¹Ï±¬ÁÏ Safety
Read Case Study
Better Control of and Access to the Safety Data
