The Industry Cloud for Life Sciences
Our industry cloud solutions provide data, software, services and an extensive ecosystem of partners to support your most critical functions from R&D through commercial. Veeva helps companies of all sizes bring products to market faster and more efficiently, and maintain compliance.
Bring Agility, Visibility, and Speed to Clinical Trials
Accelerate study timelines with modern, innovative applications.
Collect, clean, and review study data
Rapid coding for clinical terms
Manage complete and concurrent study data
Only suite of unified clinical operations applications on one cloud platform.
Vault Study Startup
Accelerate time to site activation
Stay inspection ready with active TMF
Enable proactive trial management
Pay clinical research sites faster
Vault Study Training
Streamline and automate training
Veeva Site Connect
Automate information sharing
Improve the patient experience
Learn how to prepare and comply with EU CTR.
Visit the hub
Streamline your regulatory processes, improve data quality, and respond faster to business changes with Vault RIM Suite.
Manage product registration data and changes globally
Plan, track, author, review, and approve submission documents
Vault Submissions Publishing
Enable continuous publishing and speed time to submission
Vault Submissions Archive
Securely view your complete submissions history in the cloud
Learn how to get your organization's data-ready to be compliant with IDMP requirements.
Modernizing Quality Management
Seamlessly manage your quality processes, content, and training, and provide a single authoritative source of quality information.
Gain control of GxP documents
Vault Validation Management
Manage & execute paperless validation
Vault Station Manager
Deliver right content to the right station
Ensure role-based qualification & compliance
Access accredited eLearning courses
Manage all quality process in one place
Vault Product Surveillance
Simplify postmarket surveillance for medical devices
Optimizing QC labs for real-time batch release
Building a Business Case for Quality Management Transformation.
Are you a CDMO or Generics organization? Learn More
Real-time Management of Adverse Events
Easily intake, manage, and gain real-time oversight of adverse events and pharmacovigilance content.
Collect and manage adverse event information
Centrally manage all pharmacovigilance content
Manage Signals from Detection through Risk Evaluation and Mitigation
Gain visibility into safety data with real-time reports and dashboards and seamlessly collaborate with internal /external parties.
Watch the Demo
Advancing Medical Affairs
Strengthen scientific relationships, engage experts, and deliver content in one solution built for medical affairs.
Foster informed scientific engagement across channels
Veeva Vault Medical
Streamline scientific communication through efficient content management and inquiry response
Veeva Link Solutions for Medical
Deepen engagement with real-time customer intelligence
A framework for delivering the right information to medical stakeholders in their preferred channel.
Read the eBook
Foundation for Commercial Excellence
Connected software, data, and services to advance commercial excellence for sales, medical, and marketing.
Content & Digital Asset Management
Medical Content & Inquiry Management
Veeva Crossix (U.S.-specific)
Customer Reference Data
Veeva Compass (U.S.-specific)
Strategic Advisory Services
Segmentation & Targeting Insights
Event Planning Services
Digital Events (U.S.-specific)
"Our strategic partnership with Veeva expands our capacity to leverage innovative technology and enhances our ability to deliver value to patients and all our stakeholders – this is key to how we measure success."
Chief Executive Officer and President, MSD, Read the Press Release
Connecting a Powerful Community
Become part of an active community of more than 1,100 Veeva customers
Exceed the Likely Outcome
Companies around the world are using Veeva to help change the way they do business
83% of new drugs approved
were launched with
90% faster data change
request resolution with
40% cut in TMF
reconciliation time with
50% reduction in submission
development time with