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Centralize collaborative authoring and approval, reduce risk and speed review cycles.

Study Records Collaboration

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 records
  • Author records 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 record work streams with regulatory compliance practices for record authoring, approval, control, and related training.
  • Complete the end-to-end process with electronic signature for record approvals.
  • Co-author and collaborate on new records with constant access and visibility to essential records.
  • Follow critical processes for metadata, approval, and sign-offs by publishing directly to the TMF.
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Study Record Collaboration Highlights

  • 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 Records Collaboration Capabilities

Mobile eTMF: The Pain of Yesterday.The Relief of Today.

Record Management for Clinical Trials, Quality, and Beyond

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

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Integrated with Clinical Processes

Complete the end-to-end process with electronic signature for record 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 Records or TI Clinical Study Record Collaboration room.

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