Regulations for Good Clinical Practice Article 98
The investigator should ensure the accuracy, completeness, legibility, and timeliness of the data reported to the sponsor in the CRFs and in all required reports.
中文原文 藥品優良臨床試驗作業準則第98條
試驗主持人應確保個案報告表和所有需要向試驗委託者報告資料之精確度、完整性、易讀性及時間性。