TrialFlo
IT Documentation SoftwareThis 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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