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.