Modernizing Cancer Research through Participant Data Management.

Participant-centric research solutions to address the critical gap of unifying participant-generated data with EMR, omics, biospecimens, and more.
  • Richer, more accurate data for clinical trial matching
  • Fraction of the cost of manual entry
  • Increased security and compliance
  • All-in-one integrated platform
  • Fast deployment
  • Approved by many IRBs

Data Security and Privacy Preserving Compliance With

Patient-Centric Platform to Reduce Complexity and Increase Data Quality

One of the Largest EMR Networks Assembled

1.2M+ Physicians

1.7M+ Clinical Records Integrated

3,500 Hospitals

65,000+ Practices

29,800+ FHIR Endpoints

 

Features of Vibrent's EHR-to-EDC and eSource

 

Flexible to Support Any Trial Model

 

  • Works across traditional, hybrid, and fully decentralized trials
  • Compliant for any site
  • CRO-centric model maintains consistency across sites and remote entry points
  • Access historical clinical data, regardless of patient's site

Site-Independent eSource Automation

 

  • Ingest unstructured clinical data, like physician notes
  • Completely automated - no manual data entry and no site-specific integrations
  • Flexible to support site workflows 
  • Integrate to other EDC and CTMS systems regardless of site 

Patient-Brokered Data Acquisition

 

  • Verified source data direct from EHR systems nationwide
  • Patient consents and shares data directly to the study
  • Supports remote-only and hybrid clinical trials
  • Eliminates transcription errors and data entry issues

Benefits of Vibrent's Platform for CROs

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Reduce the Number of Vendors

  • Access millions of EHR records while enabling real time patient monitoring and continuous data collection.​
  • Simplify the process to acquire EHR, wearables, RWE, ePROs, eConsent, and more into a single platform.
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Be More Competitive

  • Dramatically reduce labor cost to complete electronic data capture, and while eliminating redundancy and errors. 
  • Demonstrate ROI to clients through increased data synchronization, accuracy, and compliance.

 

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Increase Margins on Projects

  • Increase the number of clinical trials your team can manage by eliminating the slow, error-prone manual EHR-to-EDC process. 
  • Reduce rework and risk associated with errors and missed data associated with manual entry. 
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Eliminate 75% or More of Data Entry Cost

  • Research organizations using Vibrent tools can reduce the staff usage by 75% or more needed for consenting, EDC, and other data processing.
  • Enjoy the convenience of a single database across all your patient data.

Vibrent Health Is More than EHR-to-EDC:
About the All-In-One Patient Data Platform

Research Cloud
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Scale Participant Outreach, Enrollment, and Engagement

  • Achieve Your Recruitment Targets
  • Retain Participants For The Long term
  • Achieve Diversity Goals to Comply with Mandates
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Explore, Share, and Learn from Your Data

  • Real-time Data Analytics 
  • Built-in Analysis or Export to Tools like R, Python, and Jupyter Notebook
  • Export and Share Your Data Securely
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Screen and Enroll Participants Digitally

  • Capture Study Data Seamlessly
  • Easily Connect Wearables, EHR Data, and More
  • Maintain a Streamlined eConsent Experience
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Let us help you achieve your research goals with the right data and participants through compliant processes

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