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Solutions

Mednet offers a unified clinical trial platform combining EDC, RTSM, CTMS, eConsent, ePRO, eTMF, safety, and intelligent automation — empowering sponsors and CROs to accelerate study startup, enhance data quality, and maintain continuity across all stages of clinical development.

Clinical EDC

Enhance Visibility and Streamline Clinical Trial Adjudication

Clinical trial adjudication processes can be complex and lack visibility, particularly when managed with disparate systems or on paper. Our adjudication solution is different. As a seamless component of a comprehensive platform, the module provides complete visibility and is highly flexible, enabling you to adapt any adjudication workflow. 

Streamline clinical adjudication processes

With Mednet’s clinical adjudication, the Clinical Events Committee (CEC) can easily access and record critical safety data, while managing the process online with a quick glance reporting tool and dashboards that allow complete visibility to individual adverse events (AEs), adjudication results, and summary metrics. Your Adjudication Manager can easily see AEs still requiring adjudication along with those that are complete.

Improve efficiency and maximize safety with real-time adjudication

With our comprehensive eClinical platform, the adjudication committee has complete, real-time data at their fingertips. The committee has immediate visibility to events of interest, and in real-time, they can quickly and easily push requests to sites for additional information. And other key stakeholders, like the executive committee or data safety monitoring board, have the information they need to execute their responsibilities and run the trial effectively.

Remove bias with parallel adjudication and visibility

In an effort to remove bias from the clinical trial adjudication process, more and more clinical studies rely on a parallel adjudication workflow. Mednet’s adjudication solution enables teams to effectively and efficiently conduct parallel adjudication. The module supports the assignment of events, while also automatically notifying the CEC chairperson when a tiebreaking review is needed. Each committee member has access to the adjudication dashboard that provides complete event visibility, while management has access to a more comprehensive dashboard to track overall process.

The increasing regulatory pressure for independent adjudication, coupled with greater complexity in study designs and varied endpoints, makes managing the adjudication process challenging. Mednet’s adjudication solution fits every type of our required event adjudications, helping us streamline the process in studies requiring adjudication, while also providing broad visibility.

Alexandra Popma, COO, Baim Institute for Clinical Research

Everything You Need to Run Modern Clinical Trials

Design, manage, and scale clinical trials with a flexible eClinical platform that adapts to your protocol – not the other way around. Whether you’re running a single Phase I study or a global trial portfolio, our technology and experienced experts help you accelerate timelines and improve operational efficiency – so you can focus on advancing clinical research and patient outcomes.

EDC

EDC

RTSM

RTSM

eConsent

eConsent

Adjudication

Adjudication

ePRO

ePRO

Imaging

Imaging

Payments

Payments

Purpose-Driven AI

Purpose-Driven AI

Contact us for an introduction to the Mednet and CRScube eClinical ecosystem with solutions to support all study types and phases.