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Site Collaboration

Address eISF Problems and Improve Process Management with Trial Interactive Site Collaboration

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Experience the Benefits of Site Collaboration

  • Convert documents to PDF, and provide optional 21 CFR 11 Compliant Electronic Signatures within the system
  • Follow and document a Certified Copy Process
  • Redact documents, if required, directly in the system, saving time and effort

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  • Author and edit documents by opening MS Word®, Excel®, and PowerPoint® directly from the web browser
  • Track, manage, and review required documents, ensuring eISF inventory is complete

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  • Share site-facing trial documentation easily and securely
  • Use approved templates to create and collaborate on documentation - sites, sponsors, CROs, as needed
  • Use Document Version Control - Check-in/Check-out
  • Access a full audit trail
  • Use the built-in 21 CFR 11 compliant eSignature

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  • Share completed documents directly with the connected eTMF when ready, eliminating additional document capture activity

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SEE THESE FEATURES AND MORE IN A LIVE DEMO
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See How IFCT Implemented Trial Interactive Site Collaboration

Across more than 300 investigator sites, IFCT stopped printing and distributing paper amendment packages after moving to Trial Interactive eTMF and eISF Lite. The French thoracic oncology intergroup now has more reliable cross-site collaboration, stronger audit trails and fewer errors from manual document handling.

Red the ifct case study

Sick of Delays and Costly Process Management Issues? Trial Interactive's Site Collaboration can Solve Your Most Common eISF Problems

  • Save your CRAs time by avoiding on-site visits for organizing essential and source documents

  • eISF and LMS files seamlessly flow into the eTMF

  • Streamline communication with sites

  • Version control for collaborative documents

  • Make your eISF available in all required languages

  • Use controlled templates for documents to ensure compliance

  • Provide mobile access for your team members on the road

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