Veeva Unveils Innovative Cloud CTMS for Research Sites
Veeva Launches the Future of Clinical Trial Management
Veeva Systems (NYSE: VEEV) is excited to unveil its latest innovation, the Veeva SiteVault CTMS, designed specifically for research sites. This advanced clinical trial management system is engineered to enhance efficiency and seamlessly integrate with clinical trial sponsors, revolutionizing the way research teams operate.
Enhanced Efficiency with Veeva SiteVault CTMS
The Veeva SiteVault CTMS offers an all-in-one interface that allows research sites to manage clinical trials effectively. By integrating Veeva's existing technologies, such as SiteVault eISF and SiteVault eConsent, this system simplifies the management process. It enables research teams to engage in a smooth data flow with sponsors, significantly reducing manual work and improving overall operational efficiency.
Supporting Families in Clinical Research
Theresa Oswald, a leading research operations director, emphasizes the importance of efficiency in clinical studies, stating, "We need to work efficiently to help more families enroll their children in studies and get lifesaving treatment." The Veeva SiteVault CTMS aims to streamline user experiences, ultimately benefiting the patients relying on these trials.
A Commitment to Efficiency
Nick Frenzer, general manager of site solutions at Veeva, expressed enthusiasm for the release of Veeva SiteVault CTMS, saying, "High-quality cloud software and seamless sponsor integration will help sites be more efficient." Veeva is committed to making this platform available for free to more than 90% of research sites, reflecting its dedication as a Public Benefit Corporation to enhancing clinical research for both sites and sponsors.
Getting Started with Veeva SiteVault CTMS
While the initial rollout of Veeva SiteVault CTMS is slated for late 2025, it will be freely accessible for sites conducting up to 20 concurrent active studies. This initiative not only lowers barriers to entry for research teams but also signifies Veeva's commitment to making impactful tools available to those who need them most.
Live Demos at ACRP 2025
Interested parties are invited to learn more about Veeva SiteVault CTMS and view live demonstrations at the ACRP 2025 event taking place in New Orleans. This gathering will present an excellent opportunity for research professionals to see firsthand how Veeva's clinical trial management system can enhance their capabilities.
Additional Insights About Veeva Systems
Veeva Systems is recognized globally as a leader in cloud software for the life sciences sector. The company prides itself on innovation, product excellence, and prioritizing customer success. With an impressive customer base consisting of over 1,000 companies, Veeva caters to a range of clients from major biopharmaceutical corporations to emerging biotech firms.
Being a Public Benefit Corporation, Veeva is dedicated to upholding a balance among the interests of its customers, employees, stakeholders, and the broader industry. This commitment enhances the quality of services provided, ensuring they meet the evolving needs of their clientele.
Frequently Asked Questions
What is Veeva SiteVault CTMS?
Veeva SiteVault CTMS is a cloud-based clinical trial management system created to enhance efficiency at research sites.
Who can benefit from the Veeva SiteVault CTMS?
Research sites conducting clinical trials will benefit significantly from the streamlined management and data integration provided by Veeva SiteVault CTMS.
When will Veeva SiteVault CTMS be available?
The system is planned for an initial release in late 2025, with free access for sites conducting up to 20 concurrent studies.
Where can I learn more about Veeva's offerings?
For further information about Veeva Systems and its solutions, visit the official Veeva website.
Will Veeva SiteVault CTMS charge fees for usage?
Veeva has committed to providing this system for free to over 90% of research sites, promoting accessibility in clinical research.
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