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
Coming Soon
Coming Soon
Past Live Demos & Discussions
Lorem ipsum dolor sit amet, consectetur adipiscing elit, sed do eiusmod tempor incididunt ut labore et dolore magna aliqua. Ut enim ad minim veniam, quis nostrud exercitation ullamco laboris nisi.
July 2025
Strengthen Sponsor-CRO Collaboration for Greater PV Oversight and Better Outcomes
35 minutes
Gain insights on how CROs and sponsors better collaborate with real-time data visibility and direct access to a shared safety solution.
April 2025
Track Obligations and Better Manage Pharmacovigilance Agreements (PVAs) with Improved Oversight
25 minutes
See how to efficiently manage pharmacovigilance agreements and track partner obligations, eliminating manual spreadsheets, trackers, and email reminders to partners.
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.