Study Document Collaboration

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Collaboration Highlights
  • A single place to share and collaborate on clinical documentation
  • Author documents by opening MS Word®, Excel®, and PowerPoint® directly from the interface, and use the Collaborative Authoring tool for editing and review by multiple team members
  • Align document work streams with regulatory compliance practices for document authoring, approval, control, and related training
  • Complete the end-to-end process with electronic signature for document approvals
  • Co-author and collaborate on new documentation with constant access and visibility to essential documents
  • Follow critical processes for metadata, approval, and sign-offs by publishing directly to the TMF
  • Secure—Keep documents safe with secure hosting
  • Compliant—Inspection-ready audit trail
  • Efficient—Speed time to publishing
  • Collaborative—Enable multi-organization cooperation
  • Automated—Launch approved content to LMS and eTMF

Mobile eTMF: The Pain of Yesterday.The Relief of Today.
Document Management for Clinical Trials, Quality, and Beyond

With configurable indexes, workflows, document types, required documents, and dashboards, Trial Interactive provides a single place for content management. Create rooms to share and collaborate on clinical documentation for clinical trials, quality management, regulatory, and much more. TI Clinical Documents is designed to align document work streams with regulatory compliance practices for document authoring, approval, control, and training.

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Integrated with Clinical Processes

Complete the end-to-end process with electronic signature for document approvals. Follow critical processes for metadata, approval, and sign-offs by publishing directly to the TMF

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GlobalLearn Interoperability

For SOP review and approval cycles, GlobalLearn will support the capability to create mappings from content created in TI Quality Documents or TI Clinical Study Document Collaboration room