Regulations for Good Clinical Practice Article 119
The coordination approaches and responsibilities of the investigator(s) and the other participating investigators should be documented in writing prior to the start of a multicenter trial.
中文原文 藥品優良臨床試驗作業準則第119條
多機構合作臨床試驗進行前，應以書面記載試驗主持人及其他參與之試驗主持人之責任分配及協調方式。