Site Coordinating Unit

Clinical Researc Support Center

Individual-oriented on-site coordination for trial

To cope with the diversification of clinical trials and clinical studies, experienced CRCs prepare to present the trial before the IRB and communicate closely with clients, support subjects, and investigators to ensure smooth implementation of the trial. Our management of test drugs or information is strict enough for global trials or complicated protocols. We also handle serious adverse event (SAE) reports. Collaboration and information sharing with the Central Coordinating Unit and other departments of T-CReDO makes our support more practical.