Veeva CTMS

Know What’s Going On In Your Trial and Take Action Sooner

Manage trials end-to-end with a modern CTMS.

Announced 2016 Status Very Mature Customers 100+
Veeva CTMS
Find out why every biopharma needs a CTMS
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Overview

Easily manage insourced
and outsourced studies
with Veeva CTMS

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Enterprise trial management system

Veeva CTMS provides end-to-end study management and monitoring capabilities for insourced and outsourced trials.

Connected with Veeva EDC

Veeva CTMS is connected with Veeva EDC to support enrollment, monitoring, payments, and navigation to casebooks directly from within Veeva CTMS.

Full-featured to support trial needs

Dashboards and reports track key indicators, including enrollment and milestones, with drill-down to take action. Monitoring visit reports support automation and dynamic question branching. Trip reports are automatically filed within Veeva eTMF. Issues and Protocol Deviations are logged as needed and routed through resolution workflows to ensure closure. CTMS Transfer automates the daily transfer of data between sponsors and CROs using Veeva CTMS.

Impact

Centralize data and documents in one flexible system

30%

reduction in monitoring costs

50%

less time to author visit reports

80%

faster identification of issues

Why Veeva CTMS

Faster, higher quality trials

Enhance productivity

Reduce time spent on monitoring to save on trial costs.

Enable proactive decision-making

Get a 360-degree view of trial progress, automate activities, and mitigate delays to optimize trial execution.

Improve sponsor-CRO collaboration

Monitor portfolio performance to identify trends, drive impactful discussions, and enable proactive actions.

Increase compliance

Stay ICH compliant by centralizing data and documentation in one holistic system.

Customer Success

Streamlining trial management
for 200+ sponsors and CROs

Astellas Bayer Boehringer Ingelheim CSL Ferring Fortrea GSK Novo Nordisk Parelex Syneos Vertex

"The primary difference felt by study teams is they're now working in one system. When they author site visit reports, those reports automatically flow to eTMF."

Tony Lewis, Director, Trial Operations Product Owner
GSK
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"With Veeva CTMS and eTMF, we have a platform that works across the entire company with seamless integration."

John McAdory, Vice President, Clinical Operations
CG Oncology
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"We have a fully-featured CTMS and we now have proper ownership of our operational data."

Nick Kurkjy, Operational Data Project Lead for Clinical Trials
Takeda
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Resources

Explore and Learn

Read eBook
Discover why a CTMS is essential for every biopharma
Watch customer video
See how GSK simplifies site monitoring
Watch customer video
See why eTMF and CTMS are better together for Jazz
Read case study
Top 20 pharma: CTMS transformation best practices
Watch demo
Effectively plan and conduct monitoring visits
Learn more
Achieving effective study oversight with a modern CTMS
Read white paper
Modernizing the hub of clinical operations
Watch video
See how Veeva CTMS streamlines trial management
Hear from a top 20 pharma
Making the case to replace legacy CTMS

Interested in learning more?

Contact Us Download Product Sheet