Unlock the power of digital endpoints

This white paper shows how to validate, implement, and scale digital endpoints using wearables, eCOA, and AI-powered engagement—while staying aligned with FDA, EMA, and global regulatory guidance.

Clinical trials are evolving from episodic site visits to continuous, patient-driven data collection. Learn how sponsors and CROs are leveraging fit-for-purpose devices, validated algorithms, and patient-centric design to transform how evidence is generated.

Inside, you’ll discover:

  • How regulators like the FDA, EMA, and PMDA define fit-for-purpose validation
  • The three pillars of endpoint validation—technical, analytical, and clinical
  • How to merge wearable and ePRO data for richer, real-world insights
  • Operational strategies to improve data quality, compliance, and retention
  • Case studies showing how AI-driven automation reduces burden and improves outcomes
  • A quick-start checklist to design, validate, and deploy digital endpoints with confidence
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We make clinical studies virtually unstoppable

Clinical trials weren’t built for humans. We fixed that.

Delve Health turns disconnected tools into one intelligent experience—merging FDA-grade wearables, multilingual eCOA, and AI-powered engagement to reduce dropouts, improve compliance, and deliver real-time patient evidence at global scale.

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Whitepapers

eCoa
Beyond Digital Diaries — Why Delve Health’s eCOA Isn’t Just Another Vendor Solution

Learn how Delve Health is solving the challenges most eCOA vendors ignore — from licensing delays and translation gaps to caregiver support, protocol amendments, and global scalability.

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Overcoming Challenges in Wearable Data Collection

Wearables generate powerful health insights, but data quality, privacy, and integration remain obstacles. This white paper shows how Delve Health’s pipeline turns raw wearable data into reliable, research-ready insights.

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Decentralized Clinical Trial (DCT) Playbook.

This playbook provides a regulatory-aware, operationally sound roadmap for d ecentralized trials. It offers tools and frameworks rooted in real-world implementation, grounded in agency expectations, and aligned with principles of Good Clinical Practice (GCP).

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The Rise of eConsent Forms and is Impact on Patient Recruitment

Learn how to use facial recognition to ID patients, safeguard patient privacy, increase data security. and confirm ethical patient enrollment with a platform that’s HIPPA, GDPR, and 21CFRpart11 compliant.

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How Social Determinants of Health Affect Clinical Trials and What eClinical Solutions Can Do to Help Level the Playing Field

Learn more about how our innovative technology solutions can remove barriers, helping underrepresented patient populations gain access to quality healthcare worldwide.

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Revolutionizing Clinical Trials With Delve Health – A Superior Approach

In an era where the clinical trial landscape is evolving rapidly, Delve Health emergesas a beacon of innovation, offering a comprehensive and superior solution thataddresses the core challenges faced by the industry today. 

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