Regions
Europe
USA
China 中国
Japan 日本
Asia Pacific
Korea
Latin America
Industries
Life Sciences
MedTech
Consumer Goods
Chemical
Cosmetics
Collect and verify site data
Speed trial coding
Aggregate and clean study data
Randomization and supply management
Improve patient experience
Accelerate site activation
Stay inspection ready
Manage trials end-to-end
Pay clinical research sites faster
Streamline and automate training
Automate information sharing
Track global registrations
Plan and manage submissions
Publish to health authorities
Access submissions history
Gain control of GxP documents
Manage and execute paperless validation
Deliver right content to the right station
Ensure role-based qualification and compliance
Access accredited eLearning courses
Manage all quality processes in one place
Simplify postmarket surveillance for medical devices
Optimize QC labs for real-time batch release
Mitigate risk with oversight
Manage safety content
Manage signals from detection through risk evaluation and mitigation
Engage stakeholders across channels
Scientific content and inquiry management
Deeper insights, faster execution
Seamless engagement across channels
Compliant live, virtual, and hybrid events
Faster territory design & alignments
Clean, standardized customer MDM
Compliant content at scale
Data science & analytics platform
Delivers accurate data, faster
Insights on key people with Veeva Link
High quality data for U.S. life sciences
Free eRegulatory binder
Configurable eRegulatory binder
R&D, medical, and commercial solutions
Solutions from clinical to commercial
Tailored applications for animal health
Streamline content and data management
Quality and regulatory across brands
Applications to keep innovation compliant
Quality, regulatory, and claims applications
Commercial Summit, Europe
Madrid • 28-30 November, 2022
R&D and Quality Summit, North America
Boston • 19-20 October, 2022
R&D and Quality Summit, Europe
Sessions On Demand
Commercial Summit, North America
Keynotes On Demand
