Brochure | November 19, 2021


Source: TransPerfect
eclinical ctms edc

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
access the Brochure!

Get unlimited access to:

Trend and Thought Leadership Articles
Case Studies & White Papers
Extensive Product Database
Members-Only Premium Content
Welcome Back! Please Log In to Continue. X

Enter your credentials below to log in. Not yet a member of Clinical Leader? Subscribe today.

Subscribe to Clinical Leader X

Please enter your email address and create a password to access the full content, Or log in to your account to continue.


Subscribe to Clinical Leader