AI-Powered Solutions
Built by Medical Writers
For Medical Writers
TriloDocs offers specialized AI-enhanced solutions designed to enhance your medical writing workflow across the regulatory documentation submission process.
Our Approach
Our combined AI Approach Offers the Best of Both Worlds
TriloDocs uses specialized AI approaches matched to each document type in your regulatory submission workflow
Symbolic AI
• Core Technology for Clinical Study Reports
• Deterministic, non-hallucinating AI system
• Ensures accuracy and reliability in document generation
• Transparent, predictable results every time
• Perfect for processing clinical data and identifying signals
Internally AI Medical Writing Agent
• Enhanced Content Generation Across Products
• Complements deterministic AI with nuanced understanding
• Enables sophisticated content generation and translation
• Ideal for patient-friendly language and complex narratives
Clinical Study Report
Rule-Based Clinical Data Processing
Product Description
Built on our deterministic AI, TriloDocs processes your source documents with the same logical approach an experienced medical writer uses. This rule-based, non-hallucinating system rapidly identifies clinically relevant data signals, creates transparent decision pathways, and generates accurate CSR foundations - allowing you to focus on clinical interpretation rather than data processing.
Key Benefits:
• Processes source documents in minutes, not weeks
• Zero hallucination risk with rule-based logic
• Never fabricates answers - explicitly states when information cannot be determined from source data
• Transparent decision-making with customizable criteria
• Maintains regulatory accuracy and consistency
Lay Summary
Compliant Plain Language Summaries
Product Description
Built with specialized LLM-powered medical writing agents, TriloDocs converts complex clinical data into patient-friendly summaries. This specialized generative AI automatically includes all 10 regulatory components required by CTEG, while maintaining GDPR and HIPAA compliance. Delivering accessible lay summaries that meet both regulatory standards and patient needs.
Key Benefits:
• Encompasses all 10 CTEG regulatory components
• Translates complex data to accessible language
• GDPR and HIPAA compliant by design
• Eliminates compliance risk and regulatory gaps
Module 2.7.4 Summary of Clinical Safety
Comprehensive Trial Safety Analysis
Product Description
Built on TriloDocs' proven symbolic AI foundation, our Summary of Clinical Safety solution processes complex data across your entire clinical trial with the same systematic approach an experienced medical writer employs. This rule-based system rapidly aggregates data from multiple studies, identifies critical signals, parsing GIDBs, CSRs and synopsis to generate comprehensive, regulatory-compliant outputs. This platform enables your team to focus on clinical insights rather than manual data compilation.
Key Benefits:
• Summarises crucial data in minutes, not days
• Identifies clinically significant findings across all trial studies
• Maintains consistency with our expertly-designed data processing engine
• Transparent decision-making with customizable criteria