Clinical Trial Site Management Organization (SMO)
Full-Service SMO Solutions
MAVEN supports clinical trials by placing highly trained Clinical Research Coordinators (CRCs) at each research site dedicated to a specific protocol. CRCs are delegated by PI and mainly support investigators on non-medical-evaluating related study activities during the conduct of a clinical trial. CRCs are especially critical in China, as investigators are typically occupied by routine clinical work. But, many organizations struggle to resolve the shortage of human resources due to the limitations of most public hospitals in the country. Our experienced research coordinators offer diverse capabilities to conduct each clinical trial with the highest standards of quality and ethics.
MAVEN has provided full-service clinical trial SMO solutions for more than 230 clinical studies, cooperated with more than 450 sites, and managed 60,000 subjects.
Clinical Trial SMO Services for a Variety of Study Areas
We help investigators review source documents to improve accuracy, completeness, and standardization.
Welcome to Maven, one of the best Regulatory Consultants that is setup by real life working professionals with very rich experience. We at Maven understand the customers pulse and reach their expectations. We are unique and focus on quality is our prime goal. Maven works with any range of company that is looking for quality and in time delivery of services.
Welcome to Maven, one of the best Regulatory Consultants that is setup by real life working professionals with very rich experience. We at Maven understand the customers pulse and reach their expectations. We are unique and focus on quality is our prime goal. Maven works with any range of company that is looking for quality and in time delivery of services.
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