Proactive Engagement
Send friendly, automated reminders for dosing schedules, clinic appointments, and study milestones to keep patients focused.
Clinical Operations Module
AI Trial Companion for Patient Adherence
Improve patient retention and compliance throughout your clinical trials. Guide participants with protocol answers in 100+ languages, while flagging dropout risks early.
ICH-GCP Grounded
Secure HIPAA Storage
AI Trial Companion
"My clinical visit is tomorrow morning. Do I need to fast before coming to the clinic? Also, is the dosage still 10mg once daily?"
"According to your trial protocol, yes, please fast (no food or drink except water) for at least 8 hours before the visit Protocol, Sec. 4.2. Your dosage remains 10mg once daily in the morning."
Adherence Confirmed
The Trial Bottleneck
High attrition rates threaten trial timelines
Patient discontinuation is one of the leading reasons clinical trials run over schedule and exceed budgets. Site coordinators spend a significant portion of their day answering repetitive administrative and protocol questions, which delays response times and strains patient relationships.
The AI AdvantageInstant protocol guidance, 24/7
The AI Trial Companion takes the burden off coordinators by answering patient queries instantly. Grounded directly in your approved clinical trial protocols, it provides accurate, compliance-restricted answers about dosing, appointment schedules, and travel logistics in the participant's native language.
Coordinator Dashboard
Dropout Risk Alert
Risk Metric
Missed Doses (Last 14 Days)
2 Doses
Check-in Delay
0 Days
Participant Profile
#TR-7721
London Central
Moderate (Intervention Recommended)
Capabilities
Grounded Engagement for Clinical Sites
Equip your study team with compliance-aligned automation, protocol indexing, and risk metrics.
Grounded Protocol Guidance
On-demand answers to patient queries regarding medication limits, travel, and schedule details, verified by study documents.
Multilingual Compliance
Communicate with patients across worldwide multi-center trials in their local languages, maintaining strict terminology.
Attrition Risk Modeling
Analyze patient chat indicators, dose delays, and check-in speeds to alert site coordinators of potential dropout risks early.
Site Coordinator Portal
Reduce administrative burdens. Give site staff a clear workspace to monitor compliance trends and coordinate inquiries.
Regulatory Security
Ensures patient privacy with fully anonymized data handling pipelines matching HIPAA and regional clinical standards.
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