FULL PLATOFRM OVERVIEW
The Complete TriloDocs Roadmap
AVAILABLE NOW
● Dual Approach AI -Symbolic & LLM
Clinical Study Report
CSR
Symbolic AI. Zero hallucination risk. Processes source documents in minutes.
Lay Summary
CTEG Compliant
Medical Writing-guided LLM. All 10 CTEG components. GDPR & HIPAA compliant by design.
Patient Narrative
Safety Reporting
Individual patient narratives for safety reporting, generated at scale.
Informed Consent Form
ICF
AI-generated patient consent documentation aligned to regulatory requirements.
COMING SOON
Module 2.7.4 Clinical Safety Summary
2026
Comprehensive safety data synthesis across full clinical documentation, powered by TriloDocs’ dual AI system.
Investigator Brochure
2026
Comprehensive investigator information for trial sites and ethics submissions.
TriloDocs Platform
2026
Multi-user QC collaborative environment for teams working simultaneously.
Module 2.7 Clinical Summary
2026
Additional 2.7 documents: 2.7.2 Pharmacology; 2.7.3 Efficacy.
Module 2.5 Clinical Overview
2026
2.5.2 Biopharmaceutics; 2.5.3 Pharmacology; 2.5.4 Efficacy ; 2.5.5 Safety.
OUR TECHNOLOGY
The Right AI for Each Task
TriloDocs uses specialized AI approaches matched to each document type – combining deterministic precision where accuracy is non-negotiable, with intelligent generation where nuance matters.
Symbolic AI
CORE TECHNOLOGY FOR CSR
→ Deterministic, non-hallucinating system
→ Zero fabrication – states when data is unavailable
→ Transparent, auditable decision pathways
→ Rule-based logic mirrors expert medical writer thinking
→ Predictable, consistent results every time
Medical Writing Guided LLM
ENHANCED GENERATION ACROSS PRODUCTS
→ Internally trained on regulatory medical writing
→ Nuanced understanding of clinical language
→ Sophisticated patient-friendly translation
→ Handles complex narrative requirements
→ Complements deterministic AI with intelligent generation
Source Documents
TFL, SAP, CSP, CSR, GIDB, Synopsis & more
Symbolic AI Processing
Rule-based signal identification
LLM Enhancement
Intelligent content generation
Regulatory-Ready Output
Compliant, accurate documents
Clinical study Report
Rule-Based Clinical Data Processing
Built on 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.
Key Benefits
Processes source documents in minutes, not weeks
Never fabricates – states when data is unavailable
Regulatory accuracy and full consistency
Zero hallucination risk with rule-based logic
Transparent, customisable decision criteria
Statistically powered analysis of study results
Lay Sumary
Compliant Plain Language Summaries
Built with specialized LLM-powered medical writing agents, TriloDocs converts complex clinical data into patient-friendly summaries. This 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
All 10 CTEG regulatory components included
GDPR and HIPAA compliant by design
Complex data translated to accessible language
Eliminates compliance risk and regulatory gaps
Patient Narrative
Individual Patient Narratives for Safety Reporting
Generate comprehensive individual patient narratives at scale for safety reporting requirements. TriloDocs ensures consistency, accuracy and regulatory compliance across every narrative – eliminating the manual burden while maintaining the clinical precision safety reporting demands.
Key Benefits
Generated at scale across all trial patients
Meets safety reporting regulatory standards
Consistent structure and clinical accuracy
Dramatically reduces manual writing burden
Informed Consent Form
AI-Generated Patient Consent Documentation
TriloDocs automates the creation of informed consent documentation, ensuring regulatory alignment while maintaining the clear, accessible language patients require. Reduce drafting time while ensuring compliance from the first version.
Key Benefits
Regulatory-aligned consent documentation
Consistent structure across all studies
Patient-accessible language throughout
Dramatically reduced first-draft time