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

Better Oversight and Management of Pharmacovigilance Agreements (PVAs)
April 2025

Faster Literature Reviews with Keyword Highlighter
May 2025

Automate Case Processing
June 2025

Past Live Demos & Discussions

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.