Improving your ePRO solutions.

Medable Partners with Agilathon for Global Clinical Trial Delivery


With over 1,000 clinical trials, Agilathon has extensive experience in designing, developing, validating and supporting eCOA and DCT solutions. 

Agilathon is a technology agnostic services firm. Our diverse development teams build solutions that help ensure sponsors collect complete, accurate and reliable data. Read more below!

Graphic demonstrating Agilathon Scrum process. Center circle contains: Speed, Innovation, Productivity, Quality; Outer circle represents cycle of: Design, Development, Validation, Maintenance and Support.


Agilathon excels at translating your clinical trial protocol(s) into technical specifications to maximize site and patient engagement to achieve protocol outcomes.


Agilathon’s experts use an agile process to develop customized, highly-interactive, mobile-web, and other software solutions for clinical research data acquisition and management to meet our clients’ requirements.

Agilathon leverages its backend infrastructure and reporting suite to manage each clinical trial project to ensure reliable results.


Agilathon is experienced in requirements and specification analysis, test approach planning, designing and executing manual and automated test cases.

We work collaboratively with our clients in the detailed testing coverage and maintain rigorous documentation to meet regulatory standards.

Support & maintenance

Agilathon provides ongoing processes to test, adjust and ensure our clients’ clinical trial platforms continue to deliver results consistent with the protocol(s).

Agilathon validates software for each operating environment and resolves any issues rapidly with clear client reporting.


Join the Agilathon Family.

Can you have speed and endurance? At Agilathon, we think so and we can respond to time sensitive needs with a short cycle development format to deliver reliable, consistent ePRO solutions that empower researchers and doctors with the information they need to cure diseases in a more efficient way.

With offices in Split, Croatia and Cambridge, MA, we leverage time-zones to our advantage and have a well-defined process for maximizing our teams’ efficiency. For each clinical study, we create a cross-functional team, with appropriate skills to handle the project size and complexity. We work closely with the client’s project management to identify the appropriate resources and prioritize the work against other concurrent studies.

Join us and make your mark with us today!


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Our Team

About Us

We merge industry expertise in clinical trial design and implementation with the technology know-how to translate visions into reliable and consistent ePRO solutions for therapeutics.

With vast expertise and experience in designing, developing and validating software, we have contributed to many trial development projects in the patient-centered Life Sciences market.