Our Services

Expertise in clinical research.

Investigators Selection and site support

Identify and pre-qualify Principal Investigators and research sites
Prepare feasibility forms and essential documentation

Clinical Research Coordinator Staffing

Provide trained CRCs for on-site or remote study support
Flexible, project-based coordination to meet study needs

Site Initiation & Documentation

Organize site files, licenses, CVs, and logs
Set up and maintain Trial Master File and Investigator Site File

Medical/Clinical Writing & Biostatistics

Develop study proposals, reports, and patient brochures
Perform statistical analysis and data interpretation

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