Enforcement Rules for the Controlled Drugs Act Article 19

To make an initial Schedule 1 and 2 controlled drugs purchase, the institutions or businesses that have obtained a controlled drugs registration license shall ask the pharmaceutical plant under the FDA as mentioned Article 4 Paragraph 1 of this Act (hereinafter " the pharmaceutical plant ") for a specimen seal impression card that has one form with two copies. After completion, one copy shall be sent to the pharmaceutical plant, and the other copy shall be kept for reference.To purchase Schedule 1 and 2 controlled drugs, a request for the appropriate order forms shall be made to the pharmaceutical plant. After completion, the form shall be sent to the pharmaceutical plant for processing. The seal on the order form shall be identical to the one on the specimen seal impression card as mentioned in the preceding Paragraph.When the seal for the card for specimen seal impression as mentioned in Paragraph 1 is changed, one shall present the new card to the pharmaceutical plant, then one may continue purchasing.
中文原文 管制藥品管理條例施行細則第19條
領有管制藥品登記證之機構或業者第一次購用第一級、第二級管制藥品,應先向本條例第四條第一項所定之製藥工廠(以下簡稱製藥工廠)索取印鑑卡一式二份,填妥加蓋印章後,一份送製藥工廠,一份保存備查。
申購第一級、第二級管制藥品者,應向製藥工廠索取訂購單,填妥加蓋印章後,送製藥工廠申購。
訂購單上所蓋之印章應與前項送存之印鑑相同。
第一項送存之印鑑如有變更,應重新檢送新印鑑卡送製藥工廠備查,始得續購。

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