SOURCE AND ECAPTURE

Seamless data management

Let's face it, source document completion is time consuming for sites. ClinEdge's team leverages eSource and transcribes study visits into an electronic data system (EDC).

  • HIPPA/ICH-GCP Certified
  • EDC/CTMS Platform
  • Protocol/eCRF Guidelines
THE CLINEDGE APPROACH

Source and eCapture for Research Sites

The Source Development and eCapture service is carefully completed by HIPAA and ICH-GCP certified clinical research specialists, trained across multiple therapeutic areas.

Sites Leveraging eSource

Study visits are transcribed into the study’s electronic data capture system within 24 hours of visit completion. By outsourcing, site staff have more availability to meet with patients, as well as focus on the management and conduction of the clinical study.

Outsourcing Source Development and eCapture responsibilities will enable site staff to spend more time with their patients ensuring a safe, productive overall experience.

STREAMLINED SOLUTIONS

The Four Step Process

Step 1: Execute a confidentiality agreement and HIPAA-compliant business associate agreement

Step 2: Provide ClinEdge with protocol and eCRF guidelines, if available

Step 3: Grant access to the EDC management platform and site CTMS platform

Step 4: Add ClinEdge to the delegation of duties or file our note-to-file

I love getting to know my wonderful clients and seeing their research pipelines continue to thrive and stand out in a very competitive industry.

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