Pharmaceutical Good Manufacturing Practice Regulations Article 56
Where Chinese herbal medicine factories produce Chinese herbal medicine for use in clinical trials, aforesaid Chinese herbal medicine, in addition to complying with regulations governing labeling in the Act, must also be labeled “for use in clinical trials only,” and marked with the name of the party that commissioned the clinical trial and a trial code sufficient to identify the trial location and research personnel involved. However, where pharmaceuticals for use in clinical trials are tested in closed trials (double-blind trials), drug name, potency and efficacy may be replaced by product codes, serial numbers and packaging batch numbers.
中文原文 藥物優良製造準則第56條
中藥廠對於臨床試驗用藥之標示，除須符合本法有關規定外，應另標示「臨床試驗專用」、試驗委託者名稱及足以確認試驗場所、研究人員之試驗編號。
但屬非開放性試驗（雙盲試驗）之臨床試驗用藥，其應刊載之藥品名稱及藥品之含量，得以刊載產品代碼、編號及包裝批號標示替代之。
但屬非開放性試驗（雙盲試驗）之臨床試驗用藥，其應刊載之藥品名稱及藥品之含量，得以刊載產品代碼、編號及包裝批號標示替代之。