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ObvioHealth

Decentralized clinical trials powered by digital innovation and clinical expertise.

ObvioHealth delivers decentralized and hybrid clinical trial solutions through its ObvioGo platform, enabling sponsors to simplify study design, boost participant engagement, and accelerate enrollment across 40 countries. Headquartered in New York, United States.

Phases

Services

About this organization

Overview

ObvioHealth is a clinical research organization specializing in decentralized and hybrid trial management. The company operates ObvioGo®, an enterprise-grade digital platform designed to streamline clinical trial execution from protocol design through final reporting.

Core Capabilities

Study Design & Protocol Development

  • No-code, drag-and-drop interface for rapid protocol development and adaptation
  • Reduces traditional timelines by weeks

Recruitment & Patient Engagement

  • Precision digital recruitment and dynamic pre-screening tools
  • Real-time dashboards and centralized workflows
  • Accelerates enrollment by up to 4x
  • Supports reach across 40 countries and 6 continents

eConsent & Enrollment

  • Mobile-first eConsent with built-in, compliant eSignature solution
  • Investigator countersignature and participant assent support
  • Faster onboarding and higher completion rates

Data Capture & Monitoring

  • Continuous, high-quality data collection via image/audio tools, wearables, and home-based assessments
  • Real-time alerts and dashboards for informed decision-making

Patient-Reported Outcomes (ePRO + eCOA)

  • Digital capture of patient, caregiver, and clinician outcomes
  • Real-time visibility and higher compliance

Virtual Visits & Support

  • Virtual medical visits, home nursing services, and in-app clinical support
  • Improves adherence and participant experience

Logistics & Device Management

  • Unified hub for logistics, DTP shipping, and device connectivity
  • Modular architecture integrating wearables, labs, and third-party APIs

Analysis & Reporting

  • Clean, visualized, export-ready datasets
  • Patient-level trend analysis and executive summaries

Regulatory & Compliance

  • HIPAA and GDPR compliant
  • Built-in encryption protocols, audit trails, and role-based access
  • Global regulatory alignment

Experience

  • Founded 2017; 8+ years of operational experience
  • 62 studies completed (interventional, observational, and registries)
  • 50,000+ participants consented
  • Serves CRO, medical device, pharma/biotech, and consumer health industries
  • Operates across 40 countries and 6 continents
  • 15+ therapeutic areas supported

Locations

  • Headquarters

    New York · NY · USA

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