End-to-end rapid study start-up and centralized trial management designed for complex site selection needs.
With deeper integration at the site level, ClinEdge provides direct access to physicians, patients, and data that allows research to be streamlined through a managed services provider and enables recurring trial processes. This gives pharmaceutical companies a central outlet for selecting sites, managing patient study procedures, and critical data workflows resulting in flexible and adaptable study conduct, whether based in a medical system or a patient’s home.
The ClinEdge Approach
Streamlining and improving trial delivery resulting in growing efficiencies and reduced trial costs to the industry.
Rapid Study Start-Up
Site Selection & Feasibility
Streamlined Contracts, Budgets and Regulatory Compliance
Staffing & Training
Ongoing Centralized Trial Management
Enrollment Management
Compliance Management
Grant Management
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Our company’s purpose and mission has always been to improve the site and patient clinical study journey and by executing on this new category of trial support, we will help evolve the paradigm of the current trial workflow and allow for recurring processes to be realized.
