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

eSource for Research Sites

The eSource development 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.

About eSource

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


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

Our company’s purpose and mission has always been to improve the site and patient clinical study journey and by executing on this new category of trial support, we will help evolve the paradigm of the current trial workflow and allow for recurring processes to be realized.


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