eCOA completion
92–98%
Typical diary completion
Retention uplift
+40%
With layered concierge support
Global readiness
120+
Languages supported
For pharma teams running global trials
Make Your Global Trials Human.
Unified eCOA, validated wearable endpoints, and protocol-trained concierge support help pharma teams run decentralized and hybrid trials with confidence—while reducing site burden and preventing deviations early.
Cleaner evidence · Fewer missed tasks · Faster issue resolution.
The Modern Infrastructure for Global Drug Trials
Today’s trials generate millions of signals — but only actionable, validated endpoints move programs forward. Delve Health brings eCOA, wearables, and multilingual concierge together into a single, regulatory-aligned ecosystem.
- Centralized data across wearables, ePRO, and diaries
- Automated compliance with human intervention when it matters
- Regulatory-aligned digital endpoints (FDA, EMA, PMDA)
- Real-time dashboards for global oversight
Built for Pharma Sponsors
Deploy globally, validate confidently, and keep evidence flowing—Delve combines
eCOA, digital measures, consent, and analytics with a human layer that prevents drift
and missed data.
Global Scale
Deploy multilingual eCOA + wearables across any region with consistent operations.
Regulatory Alignment
Fit-for-purpose validation and documentation designed for FDA/EMA review expectations.
Human Concierge
Real humans intervene when patients fall behind—recovering syncs and preventing deviations.
Real-Time Oversight
Live dashboards for safety signals, sync failures, and endpoint quality—without waiting for exports.
Unified eCOA + Wearables
Instead of juggling siloed vendors, Delve harmonizes subjective and objective data streams into a single real-time environment.
- Validated wearable integrations (cellular + Bluetooth)
- Sensor calibration & objective endpoint mapping
- ePRO + symptom tracking with regulatory audit trails
- Digital biomarkers contextualized by real-world signals
Retention Powered by Humans, Not Just Software
When a device misses a sync, a diary goes incomplete, or a patient feels lost — automation flags the issue, and our concierge team resolves it in minutes.
- Proactive intervention for sync failures
- Multilingual patient outreach and device troubleshooting
- Scheduling, reminders, and adherence coaching
- Huge reductions in missing data and protocol deviations
Proven in Drug Development
Global Phase III Program
95% retention at 12 months with concierge + wearable oversight.
Digital Endpoint Validation
Objective signals correlated with gold-standard clinical measures.
Hybrid Oncology Study
63% improvement in adherence through patient outreach programs.
95%
Device Compliance
87%
Retention at 12 Months
60%
Fewer Missed Syncs
30%
Faster Enrollment Support
Run Your Next Global Trial With Confidence.
Real-time oversight. Validated digital endpoints. Human-centered retention.
