MedTech Solutions — Delve Health

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.

PMS
PMCF
RWE
DEV

Post-Market Workflow

Enroll → Monitor → Follow-Up → Evidence

Patient enrolled remotely. Device data and outcomes collected continuously.
Concierge ensures follow-up visits, diary completion, and device adherence.
Data reviewed in real time to support safety reporting and regulatory review.
Regulatory-grade execution Audit-ready data + documented workflows

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.

MedTech digital platform

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.

Device engagement support

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.

eCOA and device integration

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

60%

Reduction in Sync Failures

87%

Retention at 12 Months

30%

Faster Real-World Data Collection

Accelerate Your Device’s Evidence Generation.

Combine automation, wearables, and real humans in one unified workflow.

Book a MedTech Demo