eAdjudication® software serves as a hub to gather medical records directly from source systems and trial sites, preserving the quality and integrity of the data, and presenting it in a standardized, digital format.
eAdjudication® is flexible, GXP compliant, scalable, integrates easily into any data environment, and provides real-time data and event reporting.
Once your eAdjudication® multi-study platform is configured, you can easily leverage your investment to use in future studies.
Ethical keeps it simple—by design. From build and deployment to use and maintenance, the eAdjudication® software is easy to adopt, integrate, and amend.
Ethical focuses primarily on EA with a platform shaped by our staff’s experience in data management for some 300 international trials at more than 10,000 investigator sites with hundreds of thousands of patients.
eAdjudication® all-inclusive services streamline the integration and adoption of EA software throughout eClinical organizations. With data and processes freed from bias and human error, clinical trials can improve study quality, foster more reliable decision-making and save time and money.
Academic research organizations want the same benefits that larger businesses seek from EA software - the speed and lower costs that flow from more efficient work processes, more reliable data and more confident decision-making. eAdjudication® software services will deliver those benefits, plus a more flexible approach, scaled to your budget needs.
HOW WE HELP
eAdjudication® software integrates easily with your existing data management platform - quickly, flawlessly and at any stage of your program. Our software platform helps you design, manage, monitor and report with certainty on every aspect of a clinical trial required by sponsors.
HOW WE HELP
The eAdjudication® software platform streamlines the endpoint adjudication process from faster start to earlier finish. Sponsors can have more confidence in the efficient adjudication process, quality data free from bias or human error, with real-time results accessible to all authorized parties to expedite critical decisions.
HOW WE HELP
eAdjudication
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service description
In order to shed light on endpoint adjudication, the LinkedIn Endpoint Adjudication Community generated an Events Charter Template for endpoint adjudication to assist those in need of guidance.
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Are you planning to submit Endpoint Adjudication Data to the FDA or the EMA? Submitted material are not only essential for obtaining marketing authorization but also a reflection of the quality of your company’s work.
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Ethical eAdjudication® implements Guardtime KSI-Blockchain® Signature as a proof-of-evidence for data integrity and time of its eClinical Audit Trail Records.
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