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Trial Interactive

Study Document Collaboration

Centralize collaborative authoring and approval processes for your clinical study documents for reduced risk and faster review cycles.

Trial Interactive's configurable clinical document collaboration solution provides a central environment for sponsors, CROs, and investigative sites to share and author documentation for any phase of a clinical trial with a seamless flow into your LMS, study start-up, eISF, or eTMF, among other end-points. Study teams using document collaboration enjoy a more complete approach to inspection readiness, with the ability to execute and capture all document processes in a single platform. 

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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.
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We have a solution for you.

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Study Document Collaboration Features

  • 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

Study Document Collaboration Capabilities

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.

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