CRO Selects Datatrak eTMF & ePRO for $6,600,000 Contract

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Datatrak eTMF, ePRO/eCOA, and eConsent are selected after a rigorous evaluation process of various eClinical systems for a $6,600,000 CRO contract. The Datatrak eClinical Technology Platform is the only true eSource solution that seamlessly integrates ePRO/eCOA and eConsent with EDC, RTSM, eTMF, and CTMS into one user friendly dashboard with only one user login required to utilize all the key functions of data management for clinical trials. Datatrak's all-in-one end-to-end technology platform powers decentralization, hybrid, and traditional site-based clinical trials with complete flexibility and customization to meet the requirements of any study protocol. Datatrak eTMF seamlessly integrates into a central dashboard with EDC for permissions to be granted to EDC users to view documents from the eTMF, upload documents requested from the eTMF, and participate in eTMF workflows directly with EDC and other functions.

AUSTIN, TX / ACCESS Newswire / October 22, 2025 / Datatrak International (OTC:DTRK) announces a $6,600,000 commitment for Datatrak eTMF & ePRO/eCOA, and eConsent for clinical trial documentation and processes and patient centered clinical trials. The CRO will integrate Datatrak eTMF, ePRO/eCOA and eConsent into Datatrak's eClinical Technology Platform along with EDC, RTSM, and CTMS for the only true eSource solution for clinical trials. This will drive efficiency and enable better visibility across all its data management needs for study success.

Datatrak's platform is the first true eSource solution that is flexible and highly customizable to fit any protocol's needs while seamlessly integrating into one system, with one login, on one dashboard, and gives users total control over data, documents, workflows, and permissions across an entire organization globally for the key clinical trial data management solutions of EDC, RTSM, eTMF, CTMS, eConsent, ePRO/eCOA, Imaging Data, Central and Local Labs, Data Imports and Exports, Enterprise level management of Workflows and Timelines saving Life Science professionals valuable time to allow clinical operations teams to focus on driving trial results and reaching study endpoints more efficiently. Datatrak's EDC, RTMS, eTMF, CTMS, eConsent, and ePRO/eCOA beautifully integrate into Datatrak's All-In-One dashboard and allows users to manage End-to-End clinical trial data, documentation, workflows, and permissions seamlessly. The eClinical system is fully compliant with the highest Quality Assurance standards such as Part 11, HIPAA, GDPR, and other standards. , improving our overall efficiency. Datatrak is helping reduce medical device and drug development costs with technology by offering solutions that are priced much more reasonably than other eClinical vendors. Datatrak provides simple and straightforward contracts and pricing.

The Datatrak eClinical Technology Platform powered by Fountayn is the first and only true eSource solution for clinical trials enabling CROs and Sponsors to seamlessly share information and documents across EDC, RTSM, CTMS, eTMF, eConsent, ePRO/eCOA from study start-up to study closeout. Fountayn also provides an in-house dedicated and experienced full service team of trial design, project management, study support services, and help desk solutions specialists based in the United States, European Union, and Japan for better collaboration and increased efficiency throughout the study lifecycle. Schedule a demo at [email protected] and see why CROs, Sponsors, and clinical researchers are turning to the Datatrak for the only true eSource solution to optimize the entire clinical trial lifecycle.

About Datatrak eClinical Technology Platform Powered by Fountayn

Datatrak is transforming Life Sciences through technology innovations by offering the first true eSource solution platform that seamlessly integrates all aspects of clinical trial data management including EDC, RTSM, eTMF, CTMS, eConsent, ePRO, Enterprise Management Workflows and Timelines. No other eClinical company has the history of experience innovating for Life Sciences as Datatrak which has over 30 years of experience as the original pioneer of EDC and cloud software for the life sciences industry. That is why for over three decades CROs, Sponsors, and clinical researchers turn to Datatrak for a trusted, reliable, and established technology platform with the highest Quality Assurance standards that are 21 CFR Part 11, GDPR, GCP, HIPAA, CDISC compliant in a Validated Quality Management System with SOPs. See why Datatrak's technology platform is trusted in 83 countries in 6 continents with over 10,000 clinical trials. Datatrak is headquartered in Austin, Texas and our people are all based US, EU, and Japan. Datatrak does not offshore jobs and believes in creating jobs in the regions its serves. For more information, visit www.datatrak.com or www.fountayn.com.

Contact:

[email protected]

Datatrak eClinical Technology Platform Powered by Fountayn

SOURCE: Datatrak International

View the original press release on ACCESS Newswire
 

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