Pharmaceutical Affairs Act Enforcement Rules Article 23-1
The central competent health authority may engage a health foundation or other related group or organization to perform reviews of academic research, safety and clinical trials, and other technical materials in connection with the market approval of drugs.
中文原文 藥事法施行細則第23-1條
中央衛生主管機關對於藥物之查驗，得委託衛生財團法人或其他相關團體、機構辦理學術性研究、安全、臨床試驗等技術性資料之審查業務。