
Medidata CTMS
5.5#3 in clinical trial managementWeb
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| Fact | Medidata CTMS | Trial Interactive CTMS |
|---|---|---|
| Company | Medidata is a Dassault Systèmes brand, and its company history says it was founded in June 1999. | Trial Interactive describes itself as a division of TransPerfect. |
| 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. | The product page says the platform is designed to support 21 CFR Part 11, EU Annex 11, GxP, GDPR, and HIPAA. |
| Founded | 1999 | 2007 |
| Integrations | CTMS is integrated with Medidata Rave and eTMF; EDC data can populate dashboards and analysis, while uploaded documents and monitoring reports flow to the eTMF or TMF. | The product page lists integrations with EDC, IXRS, payments, eTMF, site portal, study start-up, learning management, and content management. |
| Pricing | The CTMS page directs visitors to contact a specialist to explore pricing; it does not show a price. | The CTMS page directs prospective customers to book a demo or contact sales and does not state a price. |
| Purpose | Medidata CTMS brings clinical and operational trial activity into one connected, AI-enabled solution for planning, tracking, and overseeing studies. | Trial Interactive CTMS centralizes portfolio, study, site, and subject data for planning, tracking, and reporting clinical trials. |
| 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. | Trial Interactive lists its technical Service Desk phone number as +1 888.391.5111 and email as [email protected]. |
No prices published.
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.
Trial Interactive CTMS is presented for sponsors and CROs, including CRAs, study managers, and clinical leaders. It may fit teams seeking connected planning, site monitoring, reporting, and document workflows.