Pharmaceutical Good Manufacturing Practice Regulations Article 26
Chinese herbal medicine factories shall establish detailed quality specifications for raw materials and product containers and caps, as well as operational procedures for the acceptance, labeling, storage, handling, sampling, testing and inspection of these items.Containers that hold raw materials, product containers or caps shall be clearly labeled with batch numbers and status, pending-inspection, approved for use, not approved for use, or to be isolated; this information shall be entered into the disposition record of each batch.Container caps shall, as needed, be fitted with children safety devices to prevent accidental consumption.
中文原文 藥物優良製造準則第26條
中藥廠應以書面詳訂原料、產品容器、封蓋之品質規格及其驗收、標識、儲存、處理、取樣、檢驗及審核之作業程序。
盛裝原料、產品容器或封蓋之容器，應逐批標以明確之代號及待驗、准用、拒用或須隔離之狀況，並記載於各批物品之處置紀錄。
產品容器，應視需要加裝防止兒童開啟誤食之特殊裝置。
盛裝原料、產品容器或封蓋之容器，應逐批標以明確之代號及待驗、准用、拒用或須隔離之狀況，並記載於各批物品之處置紀錄。
產品容器，應視需要加裝防止兒童開啟誤食之特殊裝置。