Regular and continuous Monitoring of Clinical Trials is essential in assuring safe subjects, quality data and a well-executed study. For every phase of clinical monitoring, ClinAsia Labs will provide to the customer in a timely regular manner, a detailed report after each completion of clinical monitoring service.

ClinAsia Labs in-house medical experts provide round the clock clinical-monitoring services and also scientific and medical support for project managing teams and investigator sites to meet strict timelines for regulatory compliance and Adverse Event  enquiry, collection, evaluation, classification, reporting and total drug safety management. Also to make sure efficient communications with client’s organization, an expert serves as your point of contact for all aspects of your study all the time.

Between various monitoring visits, ClinAsia Labs clinical research associates call investigators on a weekly basis to verify patient enrollment situation, assess study progress, reply protocol questions, discuss CRF completion and ensure the study progresses in a timely manner. Clinical Research Associates make final visits to sites to close studies after all subjects have completed or have been discontinued from the study and after all queries have been answered. This is the procedure which ClinAsia Labs employs for ensuring successful monitoring of things all through the Clinical Trial Process.