TrialFlo

IT Documentation Software

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This advanced clinical data management tool automates the creation of monitor-ready source documentation by extracting and tracing relevant fields directly from protocol PDFs within minutes, significantly reducing manual effort and ensuring accurate, protocol-specific source data. Its main features include rapid PDF parsing, extensive field tracing to original source material, compliance with industry standards such as 21 CFR Part 11 and HIPAA, and secure, compliant data handling that minimizes monitoring deviations, reduces administrative workload, and enhances data accuracy for clinical research professionals, sponsors, and site coordinators.

TrialFlo can be found in IT Documentation Software categories.

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TrialFlo Main Features

• Speed
  Creates source packets in less than ten minutes, saving weeks of work before patient enrollment.
• Accuracy
  Every field is traced back to the paragraph it came from to ensure information is correct.
• Compliance
  It helps meet security and safety standards like SOC 2, 21 CFR Part 11, and HIPAA.
• User Trust
  Trusted by many companies like Medpace, IQVIA, Parexel, PPD, and Labcorp.
• Ease of Use
  Designed to be simple, easy to use, and trusted by coordinators, investigators, and monitors.
• Time Saving
  It saves 40 to 60 hours that coordinators usually spend building source for each new study.
• Fewer Errors
  It minimizes mistakes that can be missed with hand-built source documentation.
• Monitor Ready
  It quickly creates a complete source packet from any protocol PDF in under ten minutes.
• Cost Reduction
  It reduces costs caused by manual work, lost enrollment, and avoidable errors.
• Risk Management
  Helps catch deviations and errors early, preventing costly problems during monitoring.

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