Transform raw sensor signals into validated digital endpoints. Standardize every device, operationalize every workflow, and generate continuous evidence—backed by human support that protects compliance and data quality.
Sponsors don’t just need wearables—they need digital measures that meet FDA and EMA expectations for accuracy, reproducibility, and clinical relevance.
Delve converts multi-device signals into standardized metrics and validated digital endpoints, aligned with regulatory frameworks and built for hybrid and decentralized trials.
Fit-for-purpose digital endpoint development
Correlation to gold standards
Algorithm training & verification pathways
Regulatory-aligned study documentation
Device Integration & Signal Harmonization
Connect any wearable or sensor, harmonize signals into a consistent clinical model, and keep data clean with automated QC.
Universal Device Compatibility
Connect medical wearables, consumer sensors, cellular devices, or BYOD—all in one platform.
Real-Time Signal Harmonization
Normalize HR, HRV, SpO₂, sleep, steps, and respiratory data into a consistent clinical data model.
Export harmonized endpoints directly to EDC, analytics pipelines, or regulatory submission packages.
Countries Supported
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COUNTRIES
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Devices Provisioned
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The Wearables Reality No One Talks About
Digital measures fail not because the sensors fail— but because no one operationalizes the devices.
Patients forget to charge devices. Sites are overwhelmed. CROs lack playbooks. Data gaps grow quietly.
Delve steps in with automation + real human follow-up so every wearable actually works in the real world.
Missed sync detection & human outreach
Battery, connectivity & signal monitoring
Device troubleshooting & onboarding
Site workflows & escalation paths
Global multilingual support
Digital Endpoints & Real-Time Clinical Insights
Transform raw sensor data into validated digital endpoints with live visibility into patient status, signal quality, and clinical trends.
Validated Algorithms
Gait speed, step quality, HR/HRV, sleep staging, SpO₂ trends, respiratory rate, and more.
Regulatory-Ready Digital Endpoints
Developed using correlation, training, verification, and FDA-aligned methodologies.
Live Endpoint Dashboards
Monitor patient status, signal stability, algorithm outputs, and longitudinal trends.
Endpoint + ePRO Fusion
Combine symptoms, diaries, and objective measures into unified digital outcomes.
Unified Clinical Dashboard
Endpoints, ePRO, and wearable signals combined into one clinical command center.
Digital Endpoints & Real-Time Clinical Insights
Compliance is not a reminder problem. It’s an operational one. Delve combines automation with human intervention to keep studies on track—continuously.
Human Concierge Support
Onboarding, troubleshooting, reminders, and missed sync recovery.
Automated triggers plus human outreach ensure continuous evidence collection.
95%+ Compliance
Industry-leading adherence across global, multi-device clinical studies.
Device compliance
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Retention at 6 months
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Retention at 6 months
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Validation, Deployment & Global Scale
Digital measures only matter if they are defensible, deployable, and supported at scale. Delve operationalizes validation, global device logistics, and around-the-clock study support.
FDA/EMA Aligned
Fit-for-purpose validation and reproducibility checks for digital submissions.
Provisioning & Logistics
Shipping, SIM activation, returns, replacements, and inventory management.
BYOD + Medical-Grade
Support for both patient-owned and sponsor-provided wearables.
24/7 Global Support
Technical, patient-facing, and site support teams available worldwide.
See How Digital Measures Transform Your Study
Schedule a live walkthrough of the unified platform powering sensors, endpoints, analytics, and engagement.