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| Home > Solutions > Site Management (SMO) |
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| Site Management (SMO) |
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Clinexa has unique site management capabilities. Our Site Management (SMO) work force is clinically knowledgeable, meaning
that their methods are not only innovative but also in tune with the needs of clients, patients, and investigators
and strictly compliant with the Indian and ICH-GCP.
We appoint a full-time, highly qualified clinical research coordinator at each study site to assist and support the
investigators and site staff with all study related activities, ensuring compliance with FDA, local regulatory and
ICH-GCP guidelines and an efficient completion of assigned duties. Our site coordinators have a strong personal
ethics, clinical competency, people skills, patience and flexibility. Our CRCs are dedicated, detail oriented and
have an operational knowledge of the research process and institutional infrastructure.
Our up-gradation of the research sites is a continuous process according to the study specific requirements so that
the studies conducted are streamlined with efficient site services that expedite recruitment and study execution.
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