Powering the Future of Clinical Research
Three Clicks at a Time
TriClick™ is Hill Research’s proprietary AI platform driving automation and excellence across all our CRO projects.
It embodies our belief that clinical trials can be faster, safer, and smarter, powered by human expertise and intelligent systems.
Key Benefits
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100x Faster Workflows
Automate clinical trial processes to dramatically reduce timelines and costs.
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99%+ Accuracy
Achieve unmatched precision in compliance checks, data validation, and statistical outputs.
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100% CDISC Compliance
Ensure every dataset and submission fully meets industry and FDA regulatory standards.
Our Product
TriClick™ Annotation
Automates the creation of CDISC-compliant annotated Case Report Forms for FDA submissions. Unlike manual annotation, which is error-prone and time-consuming, TriClick™ ensures consistency, compliance, and traceability across all studies. Clients benefit from faster submission readiness and reduced regulatory risk.
TriClick™ Compliance
Automatically desensitizes and anonymizes medical information to meet HIPAA, GDPR, and FDA requirements. Unlike generic data masking, it uses advanced NLP to preserve data utility while eliminating regulatory risks. Clients achieve secure, compliant workflows that withstand global audits.
TriClick™ Evidence
Extracts and synthesizes clinical insights from vast data sources, including internal trial records, medical literature, and regulatory filings. Unlike traditional manual reviews, TriClick™ delivers real-time evidence summaries to support decision-making and regulatory responses. Clients benefit from stronger scientific justification and accelerated submission strategies.
TriClick™ Stats
One-click statistical programming tool that generates TLFs (Tables, Listings, Figures) by integrating SAP logic and SDTM/ADaM datasets. This eliminates manual coding errors and improves reproducibility. Biostatistics teams can deliver validated outputs up to 70% faster, ensuring consistency and audit-ready submissions.
AI Capabilities
TriClick™ powers Hill Research’s CRO services through six core AI agents that automate, validate, and accelerate the entire biometrics workflow, from raw data management to regulatory submission.
LLM-Augmented Clinical Analytics System
Data Compliance Agent
Evidence Summary Tool
Data Management Platform
Data Reverse Engineering
Relational Information Extraction
Why Choose TriClick™
Accelerate Biometrics Workflows
TriClick automates critical tasks — from annotation and table generation to statistical programming, delivering up to 100x faster workflows with 99%+ accuracy, while reducing manual programming by 82%.
Ensure Regulatory Excellence & Data Integrity
AI-driven compliance agents validate outputs in real time, ensuring 100% CDISC-compliant datasets and smoother FDA submissions with fewer rework cycles.
Shorten Development Timelines & Improve Collaboration
TriClick strengthens operational efficiency across clinical teams, accelerating TLF delivery by 70% and enhancing coordination across functions, ultimately increasing the probability of regulatory success.
“TriClick™ brings the power of agentic AI into our clinical trials practice, practical, precise, and ready for today’s regulatory standards. By automating critical workflows and ensuring compliance by design, it gives sponsors not just faster results, but the confidence to move forward in an era where the FDA is opening the door to AI-driven innovation.”
CTO Jack Li on TriClick™
Talk to our AI Expert
The FDA is embracing AI. So should your trials. Book a consultation with our Clinical AI Solutions Consultant and discover how TriClick™’s agentic AI can deliver faster, safer, and more compliant results for your next study.