Medidata CTMS
5.5#3 in clinical trial managementWeb
VisitMedidata CTMS vs SiteVault CTMS
SiteVault CTMS
6.8#1 in clinical trial managementFree planFree planAndroidiOSWeb
VisitWhat both publish
| Fact | Medidata CTMS | SiteVault CTMS |
|---|---|---|
| Compliance | Medidata lists documentation addressing regulations including ICH E6, 21 CFR Part 11, EU GMP Annex 11, and FDA guidance, with some materials requiring an iMedidata account. | SiteVault states that it is GCP, HIPAA, and GDPR compliant and CFR Part 11 validated. |
| Founded | 1999 | 2007 |
| Headquarters | New York, New York, United States | Pleasanton, California, United States |
| Purpose | Medidata CTMS brings clinical and operational trial activity into one connected, AI-enabled solution for planning, tracking, and overseeing studies. | SiteVault CTMS supports trial management from pre-award budgeting and visit scheduling through post-award invoicing and payment reconciliation. |
| Support | Medidata Professional Services provides enablement beyond implementation to help teams adopt and optimize CTMS, and the company offers self-paced and instructor-led training. | SiteVault includes on-demand 24/7 global support at no cost; the FAQ describes phone, email, and chat support and training at no cost. |
Medidata CTMS plans
- Medidata CTMSPriced on request
SiteVault CTMS plans
- SiteVault FreeFree
- SiteVault EnterprisePriced on request
Pick Medidata CTMS if…
It suits clinical research teams managing sponsor-led or CRO-managed studies that need trial workflows, monitoring, enrollment forecasts, and cross-study analytics in one system.
Pick SiteVault CTMS if…
SiteVault CTMS suits clinical research teams that need to coordinate studies, participants, visits, and study finances. The free plan may suit teams managing up to 20 concurrent active studies.