Document Generation
The Imperative for Automated Document Generation Systems
Clinical Trial Documentation

The Document Generator aids in writing, reporting, and regulatory compliance. The features include (1) Template-Driven Documents, (2) Built-In Regulatory Guidance, (3) Automated Data Population, (4) Version Control and Audit Trails, (5) Secure Access and Permissions, and more.

Features
Text Generation (SoA, Summary, Abbreviation) Text Conversion (AMA style guide, Tense, Lay language) Text Classification Translation Critiquing Content (Comparing to guidelines) Structured Data Generation (Table, Diagram, Chart)
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Why

1. Efficiency in Document Creation
The tool drastically cuts down the time required to draft trial documents. This increase in efficiency allows clinical teams to concentrate on trial design and execution.
2. Assurance of Compliance
FDA compliance is non-negotiable. The Document Generator provides that assurance. It reduces the risk of non-compliance-related trial delays.
3. Improved Data Integrity
With automated data population, the integrity of the reported data is solidified. Accurate reporting is vital in trial documentation.



MPilotAI
AI Copilot for Clinical Trial Design