Protocol-driven eSource

An Electronic Health Record built for clinical research.

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Overview

A protocolarized eSource that captures source data contemporaneously and consistently, eliminating transcription errors and producing ALCOA++-compliant records from day one.

Key features

  • Protocol-specific forms per study
  • Contemporaneous source data capture
  • ALCOA++ and FDA 21 CFR Part 11 compliance
  • Legal and regulatory validity of every record

Benefits

  • Fewer transcription errors
  • Audit-ready data

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