Replace error-prone paper handbooks with Clinion eSource, a digital solution for capturing participant data directly at the source. This guided walkthrough demonstrates how our role-based process enhances data integrity and control during on-site patient visits.
Your instant access includes guided walkthroughs for:
- The Investigator or CRC: Learn how site staff initiate the process by logging into the eSource application on a tablet and providing it to the participant during a site visit.
- The Subject or Participant: Discover how the participant (the only person who can enter data) is guided to complete all required fields and validates their information with a digital signature for submission.
Take ePro Product Tour
Awards & Recognitions
Achievements in Clinical Excellence
Clients Testimonials
What Our Customers Say About Our Services
“ We didn’t think setting up a study in two weeks was possible until we used Clinion’s EDC. It’s intuitive, well-designed, and feels like it was built just for us. If you're looking for an innovative, robust EDC that truly supports you, this is it.
“ Clinion EDC combines a strong product with reliable support, which has been essential for our studies. It is robust and easy to navigate, with features like the visit scheduler and data loader that make our workflows better and efficient.
“ I have to say that the team and database are AMAZING!!
“ The Support team is very cooperative and available as and when required.
“ Clinion’s software is simple to configure and understand.
“ The ease and speed at which a new study can be set up in Clinion is commendable. We can set a study up within two weeks.
“ Clinion's EDC is one of easiest and quickest solution for building and configuring studies.
Let’s Accelerate, Simplify, and Succeed in Clinical Trials Together!
Discover how leading research teams reduced inefficiencies and improved data quality with Clinion eSource
Compliance
Fully Compliant with Global Standards
