Regulations for Good Clinical Practice Article 120

When conducting a multicenter trial, all investigators should comply with a uniform set of standards for the assessment of clinical and laboratory findings, and on completing the CRFs.
中文原文 藥品優良臨床試驗作業準則第120條
進行多機構合作臨床試驗時,所有試驗主持人應遵從一致之標準評估臨床結果、實驗室結果及填寫個案報告表。

English translation for reference only; the Chinese text prevails. Not legal advice.