Redefining CTMS for Sites
Reduce manual effort maintaining trial data.
SiteVault Clinical Trial Management System (CTMS) was designed specifically for research sites and is unified with SiteVault eISF and eConsent.
SiteVault CTMS allows investigators to capture and track patient activity throughout a trial from scheduling study visits and procedures to generating invoices and tracking payments.
A CTMS does not have to be yet another hard to use system. Veeva reduces the manual effort site’s use maintaining and re-entering data.
Why Choose SiteVault CTMS?
Free For 90% of Sites
SiteVault CTMS is free for sites running less than 20 studies. Upgrading to SiteVault Enterprise beyond 20 studies is easy and affordable.
Unified with SiteVault eISF and eConsent
Save time by entering shared information like users, study team roles, research participants and general study details only once across the eISF and CTMS.
Integration with Veeva Sponsors
Over 450 sponsors use Veeva to connect with 10,000+ study sites. SiteVault enables sites to seamlessly integrate with sponsors to streamline information sharing and speed trials.
Performance & Scalability
SiteVault CTMS is designed for optimal performance and effortless scalability, ensuring it can handle growing demands while maintaining speed and reliability.
Ease of Use
SiteVault CTMS does not require users with specialized training or roles to maintain the system. Study calendar builds are simple and do not require outsourcing.
Onboarding & Support
Get started on day one without the requirement of professional services or additional fees. SiteVault comes with technical support offered 24/7 from an experienced global team.
So What's Next?
While our CTMS won’t be available until August that doesn’t mean you have to wait to see it!
Sign up below to stay up to date on the latest additions and key dates as we countdown to launch day.
Interested in becoming an early adopter? Click the demo button in the form below to begin.
Sign Up To Stay In The Know!
