Clinical Monitoring

One core support provided by CDSA is in clinical monitoring. Clinical monitoring ensures that all systems followed during study conduct are as per international ethical and scientific quality standards which include but are not limited to ethics approvals, compliance with ethics approval terms, adherence to protocol, participant recruitment process, seeking informed consent from participant, investigational product management, randomization procedures,  recording protocol deviations as per regulations/ guidelines, ensuring meetings of the data and safety monitoring boards with reports and recommendations, safety reporting, issues related to compensation and processes to be followed for site closure, premature termination or suspension of trial. CDSA has been instrumental in conducting clinical monitoring for several projects as listed on the project section of the website.