Open Source EDC: ClinCapture®
With over 11,000 users, clinical open source EDC systems are a strong example of the tremendous value clinical open source software can bring to the clinical trial process of pharmaceutical, biotechnology and medical device companies. Our open source EDC system, ClinCapture®, is particularly suited to the needs of life science companies that must reach clinical decision points efficiently and at a lower cost.
Contact us to find out how we can help you increase the performance of you clinical trial!

An easy-to-use, fully validated open source EDC platform, to run efficient clinical trials
We validated and enhanced the #1 open source EDC platform to develop ClinCapture®. Fully customizable to your clinical study, ClinCapture is an open source EDC platform that delivers the same benefits as proprietary EDC systems with no license fee. Clinovo continuously develops new features to ClinCapture to deliver an improved clinical trial design. Download our ClinCapture Datasheet
ClinCapture, greater functionality at lower costs
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ClinCapture has been successfully implemented for major biotechnology and pharmaceutical companies.

Sophisticated enhancements to the #1 open source EDC platform
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Our Open Source Technology Expertise
At Clinovo, we believe that sharing technology can bring medical innovations faster to patients. As such, we have been early adopters and strong proponent s of open source technology. By developing open source software for clinical trials, we expand the access to clinical systems, for they require no license fees while keeping high clinical data quality and security. Read more
Our EDC Expertise
Our Electronic Data Management team is experienced in designing, building, and conducting studies using leading EDC systems, including Medidata Rave®, OpenClinica™ and Oracle™ Remote Data Capture (RDC).
Leveraging our unmatched technology and IT knowledge, we streamline your Electronic Data Capture process and help you increase the performance of your clinical trial. Our certified EDC experts can implement and customize roles, workflows, and eCRF features for any clinical study, no matter its complexity, to help you avoid human error during clinical data collection and assess your clinical data quality at an earlier clinical trial stage. Read more



