THE OLD WAY

Complex internal processes required to determine event and endpoint outcomes can slow down your trial's progress and result in compounding discrepancies downstream.

THE JUDI WAY

By harnessing the 100% configurability of Judi for Adjudication, trial sponsor and CRO teams are able to rapidly deploy automated software-guided workflows matched to your internal processes that expedite review and offer complete visibility into critical study information and events globally, and in real-time.

Key Features

A Unique Solution for Endpoint Adjudication

Judi for Adjudication is designed from the ground up to support investigator sites, CROs, data managers, CEC members and sponsors who submit, collect, manage, organize and adjudicate clinical endpoint data.

Your Adjudication Workflow

Adjudication is a collection of your unique workflows applying to different event types, organizing activities and optimizing tasks while ensuring the quality of data in the system. Stakeholders can concentrate on analysis while Judi handles the management of the entire process.

Intuitive Interfaces for Investigators

Trial coordinators benefit from an intuitive interface that facilitates the collection, de-identification and submission of event-specific documents for review and dossier aggregation. A powerful query management system with configurable notifications and reminders ensures that tasks don’t linger and processes can move efficiently.

Global Views for CRO Reviewers & Data Managers

Trial managers take advantage of a global view of all their projects, seeing at a glance the state of every event in the system. With an ability to communicate directly with sites, adjudicators, and committees, CROs can keep track of their entire endpoint adjudication workflow, enabling them to keep processes running efficiently.

Enabling Adjudicator Collaboration

Adjudicators benefit from robust dossiers which are easy to navigate. With access to advanced eCRFs that enable them to perform evaluations, vote or request additional information from trial managers, these key opinion leaders can work asynchronously while Judi keeps track of all their activities.

We offer customized and concise virtual demonstrations of Judi.

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CASE STUDY

Judi delivers crucial adjudication for ICON under tight deadline

Problem

ICON’s Independent Data Monitoring Committee & Event Adjudication group needed an electronic adjudication system to support a client’s urgent deliverable for regulatory submission. Two separate, identical, customized electronic adjudication system databases were required to support adjudication of 800 events, across two programs, and 99 individual protocols. All event adjudication activities and data deliveries needed to be completed within six weeks.

Solution

The ICON team selected AG Mednet’s Judi, a web-based, regulatory-compliant, controlled, customizable electronic adjudication system, that provides transparency of end-to-end adjudication processes for each event. AG Mednet’s experts provided collaborative support to both the ICON Data Monitoring Committee & Event Adjudication team and its client, accurately capturing database requirements and reporting. AG Mednet swiftly completed all programming/validation activities, and delivered the customized Judi databases within one week, ready for event adjudication.

Result

Judi’s intuitive navigation and simplified user experience allowed the ICON team to efficiently complete adjudication of all 800 events and deliver results to the client within the six-week timeline. The established relationships and professional collaboration were instrumental in meeting this timeline.

Download the ebook to learn more about how Judi optimizes adjudication workflows!

Judi for Adjudication is designed from the ground up to support those who submit, collect, manage, organize and adjudicate clinical endpoint data, such as:

• Investigator sites
• CROs
• Data managers
• CEC members
• Sponsors

See Judi in Action; Request a Demo today

Contact us today to learn more about how Judi can automate, expedite, and improve your clinical trials.

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