Discover how to Transform Safety at
World Drug Safety Congress
Join Veeva at World Drug Safety Congress to learn how modern solutions can help you achieve greater operational efficiency and empower your safety teams with more insightful data.
10:45 am
Discover how safety teams are automating post market case processing globally. See a demo of low touch case processing and seamless adverse event intake from Vault MedInquiry.
11:50 am
Speakers:
Lisa Reeber, Associate Director, Patient Safety IT Lead, Merck
Mike Kruczek, Senior Director, Vault Safety, Veeva
1:40 pm
Learn how small biotechs can evaluate and rapidly implement a new safety solution in just 8 weeks.
Moderator:
Christina Kim, Senior Director, Vault Safety Strategy, Veeva
5:45 pm
See multilingual local ICSR reporting in one global pharmacovigilance solution including submissions to PDMA (Japan), FDA, MHRA, and EMA. Easily track and view all ICSR submissions globally.
10:45 am
See how to easily collaborate across internal and external parties while centrally tracking and managing pharmacovigilance agreements and obligations.
10:55 am
Streamline core/local risk management plan (RMP) authoring, maintenance, and tracking. Easily identify current content with version management and track implementation of aRMMs for improved compliance.
Connect with Safety Leaders and Experts
Visit booth 431 to connect with industry leaders who are advancing patient safety.
See how you can empower your organization and accelerate digital PV transformation with Veeva Vault Safety.
3,000+ / Day
Cases processed |
20,000+ / Year
Low-touch cases processed |
60+ PSMFs
Managed globally |