Live Demo Series
Drive Drug Safety Innovation with Veeva Safety
Hear from product experts on the latest safety capabilities and best practices.
Upcoming Live Demos & Discussions
Join a live demo and discussion on how to efficiently manage pharmacovigilance agreements and track partner obligations.
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Past Live Demos & Discussions
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March 2025
Automate End-to-end Clinical Patient Safety for Improved Efficiency and Data Quality
25 minutes
See how to automate information flow between clinical and safety teams to streamline case processing of serious adverse events (SAE) and distribution of safety letters.
January 2025
Improve Oversight and Efficiency in Global Risk Management
25 minutes
Learn how to reduce compliance risks related to risk management and efficiently collaborate across global and local teams/affiliates.
August 2024
Accelerate Owning Your Solution Safety Solution and Get Real-time Data Visibility
20 minutes
Discover how emerging biotechs can support case processing, ICSR submissions, and operational reports and dashboards with an out-of-the-box safety solution in only 8 weeks.
June 2024
Streamline Multilingual ICSR Reporting with One Global Safety Solution
20 minutes
See how to directly support multilingual local ICSR management and submissions to global health authorities that include PMDA (Japan), MFDS (Korea), NMPA (China), FDA, MHRA, and EMA.