Regulations for Good Clinical Practice Article 38
The investigator should ensure that all persons assisting with the trial are adequately informed about the protocol, the investigational product(s), and their trial-related duties and functions.
中文原文 藥品優良臨床試驗作業準則第38條
試驗主持人應確保所有試驗相關人員對試驗計畫書及研究藥品充分了解，以及其於臨床試驗中之責任與工作。