CCeSource

Increase data accuracy and quality.

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CCeSource

CCeSource is a comprehensive electronic source data system that enables study workflows to easily capture source data in real-time, speeding up capture time, minimizing duplicate data entry, reducing monitoring visits and optimizing site data operations.

The ability to remotely share high-quality, digital data reduces sponsor monitoring costs and speeds up source data verification, enhancing your chances of being selected as a site. Many sponsors are also happy to cover your eSource costs! CCeSource elevates the quality of the information captured, minimizing study delays and allowing more time with patients.

CCeSource

Why CCeSource ?

Data Entry

Reduces Data Capture Time

  • Provides efficient digital capture
  • Minimizes double-data entry
  • Enables mobile device access

Quality

Increases Source Data Quality

  • Provides built-in edit checks and QA workflows
  • Enables real-time query resolution
  • Reduces protocol violations

Collaboration

Minimizes Monitoring Visits

  • Improves site/sponsor relations
  • Enables remote monitoring and verification of data
  • Increases quality of shared data

Reduce Time

Reduces Payment Cycle Time

  • Allows for faster payments
  • Speeds up source data verification
  • Increases data accuracy

Integration

Streamlines Data Access

  • Provides efficient digital capture
  • Allows access from mobile devices
  • Empowers remote monitoring

Financial Performance

Enhances Study Financial Performance

  • Reduces study billing cycles through real-time reporting
  • Minimizes transcription errors
  • Allows remote post-visit tasks

Clinical Research Resources

CCeSource
Blog Post
The COVID-19 pandemic has caused an enormous disruption in healthcare priorities and staffing, and as restrictions on people’s movement have increased, clinical research sites face unprecedented challenges to adjust studies and patient engagement accordingly. The FDA has provided guidance to support ongoing continuity and response efforts, wherein the safety of trial participants is paramount. It […]

Increase data accuracy and quality.

Request Demo