Patient retention
With human-led follow-up
Data completeness
High
Wearables + ePRO + devices
Regulatory readiness
PMS / PMCF
EU MDR · FDA · Global
Post-market clinical trials & real-world evidence
Accelerate Real-World Evidence After Approval.
From post-market surveillance to long-term device performance, Delve Health supports medical device studies with unified data capture, human engagement, and real-time oversight—so evidence is reliable, defensible, and submission-ready.
Designed for post-approval studies, registries, and long-term follow-up.
The New Standard for Device-Driven Research
Whether you’re launching a new device, conducting usability studies, or generating real-world performance data, Delve Health gives MedTech teams a unified digital backbone — combining eCOA, wearables, device telemetry, and concierge support into one coordinated workflow.
- Post-market clinical follow-up (PMCF) automation
- Device monitoring + symptom diaries
- Patient training and troubleshooting via concierge
- Real-time data visualization for product teams
Built for Medical Device Companies
From post-market follow-up to real-world performance monitoring, Delve supports
medical device teams with validated data, global deployment, and human-backed
compliance.
Post-Market Studies
Rapid deployment for PMCF, vigilance, and real-world evaluations.
Device Training
Patient and clinician education with reminders, videos, and live support.
Wearable Integration
Seamless connection to cellular and Bluetooth-enabled sensors.
Real-Time Insights
Monitor device performance, adherence, and signal quality live.
Data From Devices Needs People Behind It
Devices don’t always sync, batteries die, and users make mistakes. That’s why Delve pairs automation with a multilingual human concierge to ensure every device performs — and every dataset stays clean.
- Proactive outreach for sync failures
- Step-by-step device troubleshooting
- Compliance coaching and reminders
- Daily monitoring of device health + signal quality
Unified eCOA + Device Workflows
Replace complex, multi-vendor setups with a single ecosystem that brings together symptom diaries, device telemetry, video training, visit reminders, and regulatory audit trails.
- Device telemetry synchronized with ePRO/eCOA
- Automated alerts for abnormal signals or inactivity
- Visit scheduling, reminders, and follow-ups
- End-to-end audit trails for compliance
Proven With Leading Device Manufacturers
Post-Market Respiratory Device
Visits reduced from 12 → 2 using remote monitoring.
Implantable Device PMCF
71% improvement in compliance using concierge support.
Wireless Sensor Study
38% reduction in missing data with automated alerts.
95%
Device Compliance
87%
Retention at 12 Months
60%
Reduction in Sync Failures
30%
Faster Real-World Data Collection
Accelerate Your Device’s Evidence
Generation.
Combine automation, wearables, and real humans in one unified workflow.
