TI CTMS

Read about how TransPerfect's CTMS can bring studies live in less than 30 days, while being the solution for study managers and CRAs that focuses on monitoring requirements.

CTMS Highlights

• Author-to-Archive Site Portal to eTMF
• Mobile CRA Monitoring App for Visit Reporting
• Visual Reporting and Configurable Dashboards
• Clinical Portfolio, Program, and Product Management
• Sponsor, Site, Vendor, and Lab Management
• Country and Region Management
• Activity Plans with Milestones
• Subject and Subject Visit Management
• Letters and Report Creation
• Better Data Quality through Standard Business Practices
• Protocol Deviation and Issue Tracking
• Clinical Trial Performance and Reporting
• Flexible Support for Many Trial Designs
• Built-In, Best-In-Class Content and eTMF
• Site Activation and Study Start-Up
• Configurable Reports with Custom Fields
• Document Workflows with eSignature Approvals
• Powerful Web Services and Digital Interoperability
• EDC, IXRS, and Payment Integrations
• 21 CFR Part 11 and EU Annex 11 Compliant