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End-to-End Clinical Trial Management

Full-Service Research
We handle everything from study design to final analysis using our proven, collaborative systems.

Core Services:

Comprehensive regulatory oversight, including IRB and ethics coordination

Thorough participant monitoring, adverse event tracking, and regular health evaluations

Advanced data systems: incorporating SOMS, CTMS, and EDMS (replacing EDC)

Customized study design in partnership with sponsors, tailored to each study's goals

Experience in supporting large-scale and government-sponsored trials

Full-Service Research Support, from Grants to IRB Approval

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