Brochure | September 11, 2019

TI Clinical Content Collaboration: Simplify Clinical Document Lifecycles

Source: TransPerfect

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.

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