TI Clinical Content Collaboration: Simplify Clinical Document Lifecycles

Sponsors, CROs, and investigative sites around the world can centralize clinical content processes, oversight, quality management, submissions, and compliance for speed and reduced risk.

• Expedite document creation & approvals
• Enable effective oversight
• Forecast approvals & submissions
• Simplify entire document lifescycles
• Automate processes & audit reporting
• Improve stakeholder collaboration
• Seamlessly publish to eTMF
• Seamlessly publish to LMS
• Improve quality management
• Activate real-time inspection readiness

End-to-end document lifecycles that publish directly to the eTMF and LMS, creating cultures of inspection readiness and operational excellence.