AI-Enhanced
Medical Writing Solutions
Created through collaboration between medical writers and AI engineering specialists, for medical writing professionals. We dramatically reduce regulatory medical documentation creation time, enabling your clinical teams to deliver compliant documents faster, while focusing on strategic clinical insights.
Signal Identification
Handles the heavy lifting (data deep-dive) of error-free data processing so medical writers can concentrate on clinical interpretation and strategic messaging.
Rapid Data Processing
Processes source data in hours, instead of weeks, with flexible workflows that adapt to your study requirements, highlighting clinically relevant findings so you can quickly understand what the data is telling you.
Compliant Document Generation
User instructed and AI-powered creation of regulatory-ready initial drafts that incorporate compliance requirements and quality standards from the first version.
Trusted by Global Pharmaceuticals, Biotechs & CROs
“The Flowchart for participant disposition that TriloDocs created was alone worth the price.”
- Senior medical writer with 7 years experience at a major Pharmaceutical company.
“We compared the TriloDocs output to a final CSR that we had prepared and TriloDocs found a clinically relevant safety finding that we had overlooked.”
- Clinical researcher at Medium-sized Pharmaceutical company.
“Even if I’ve already written the first draft of the CSR, I would still want to run the data through Trilodocs to check and see if the findings I identified were correct and if I have all the data. It just gives me that peace of mind to know I haven’t missed anything.”
- Senior Director of Medical Writing, at top 10 CRO with 10+ years experience in regulatory medical writing.