SiteVault CTMS

SiteVault Clinical Trial Management System (CTMS) is a solution tailored for research sites, offering integration with SiteVault eISF and eConsent features. It facilitates investigators in capturing and monitoring patient activity throughout clinical trials, from the scheduling of study visits and procedures to the generation of invoices and the tracking of payments. This system minimizes the complexities traditionally associated with CTMS tools, lessening the manual effort involved in maintaining and re-entering data.

Key Benefits of SiteVault CTMS:

• Complimentary for sites managing fewer than 20 studies, with an easy and cost-effective upgrade to SiteVault Enterprise for larger studies.
• Saves time by allowing shared information such as users, study team roles, research participants, and general study details to be entered only once across both eISF and CTMS components.
• Facilitates seamless integration with sponsors to streamline data sharing and accelerate trial processes, with over 450 sponsors connecting more than 10,000 study sites.
• Designed for high performance and scalability, handling increased demands while maintaining speed and reliability.
• No specialized training or roles are required for system maintenance, simplifying the process of building study calendars without outsourcing.
• Immediate setup without the need for professional services or additional fees, supported by 24/7 technical assistance from an experienced global team.

For further insights, download the CTMS Product Brief, and stay updated on new developments by signing up for notifications. A demo option is also available for those seeking an in-depth understanding of the capabilities of SiteVault CTMS.