REMOTE MONITORING ELECTRONIC SOURCE PLATFORM

Remote Monitoring Electronic Source Platform

ClinEdge’s Remote-Based Monitoring Platform utilizes a site electronic source and regulatory system that can be interfaced within a sponsor's clinical trial platform. In addition to being Part 11 compliant, this platform allows for easy access to each site’s source documents, query management, and direct communication between site staff and monitor. This platform will allow for increased study visibility and eliminate paper-based documents.

  • eSource Technology Integration
  • Remote-Based Monitoring
  • Rapid Startup
REMOTE MONITORING ELECTRONIC SOURCE PLATFORM

Making your trial more accessible

ClinEdge offers a unique service that can be added to manage and oversee remote-based monitoring of clinical trials. Paper source can be managed through our portal and new trials can be launched leveraging the already-established site eSource platform, thereby effectively minimizing the onboarding timeline.

eSource Technology Integration

Easy access to site’s source documents through the use of eSource technology at the site level

Remote-Based Monitoring

Direct communication through the portal between site and monitor

Rapid Startup

Sites are able to startup quickly and receive CRA training with ongoing support

REMOTE MONITORING ELECTRONIC SOURCE PLATFORM

Multiple Options to Fit Your Trial’s Needs:

Enterprise Level

  • Protocol Review
  • Source Built Based on Requirements
  • Site Training on eSource
  • Weekly Reporting

Prime Level

  • Training on Remote-Monitoring Platform
  • Customized Templates Built Based on Study Source
  • Site Training on eSource
  • Weekly Reporting

REMOTE MONITORING ELECTRONIC SOURCE PLATFORM

Compliance:

Meets strict GDPR requirements

Part 11 compliant

Access to a global compliance team with expertise in each country’s local laws

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