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  • Services

  • The following are some of the services the OSCCC provides its sponsor and study sites:

    • Design of clinical protocols by experts in critical care, infectious disease and biological defense
    • Assistance with accurate execution of protocols
    • Participate in meetings between sponsors and regulatory authorities regarding protocol design
    • Enrollment approval of all study participants conducted by five OSCCC physicians, ensuring a homogenous study population
    • 24-hour interpreter service to ensure precise translation, thus consistent patient enrollment
    • Full-time research program manager who oversees all OSCCC processes
    • Monitoring of study sites to ensure adherence to trial protocols
    • Interpretation of data
    • Analysis of the clinical trial process
    • Maintain electronic documentation of all interactions with study sites
    • Site selection and review
    • All activity performed within the Food and Drug Administration and the International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use guidelines.