Clinical Study Support

CDSA collaborates with Government Agencies and Institutions, Academic Institutions, and Small and Medium Enterprises (SMEs) in coordinating and/or implementing their clinical studies. A broad range of skills offered by CDSA include: regulatory consultation, project management, clinical monitoring, medical writing, safety monitoring, audit, data management and biostatistics support.

Department of Clinical Portfolio Management (CPM) in CDSA has been established to support investigators/ academic institutes/ SMEs in planning, site set up and initiation, conduct, project management,  data management, establishing data and safety monitoring committees for the trial and quality management. The specific studies/trials and the role of CDSA in each are detailed in projects section of website.