Clinical Trial Conduct & Management

Product description

Prior to the conducting of the clinical trial, the study must be approved by the Research Ethics Committee. Then a Site Initiation Visit (SIV) will be performed and the clinical staff (Medical Doctor, Research Nurses, Clinical Trials Assistant, Nutritionist, Research Technician etc.) will be updated on all aspects of the study. Our services include subject recruitment and screening, study conduct, electronic data capture, data and quality management and independent study monitoring.
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