Enforcement Rules of Veterinary Drugs Control Act Article 5

The competent authority may delegate its subordinate authorities, or commission administrative authorities with no relationship of administrative subordination, juristic persons or private entities to exercise a part of its powers for the following matters:5.1 Testing and registration in Article 12 of the Act.5.2 Changing the entries on registration in Article 13 of the Act5.3 Renewal of veterinary drug license in Section 14.1 of the Act.5.4 Sampling and inspection in Article 18 of the Act5.5 Inspection of veterinary drug manufacturer in Article 25 of the Act.5.6 Inspection of an entity (a veterinary drug manufacturer or dealer, veterinary care facility, farm of livestock, poultry or aquaculture, feed manufacturer or veterinary drug user, and sampling and testing of its veterinary drug in Article 26 of the Act.5.7 Sampling and testing of suspicious counterfeit, banned or substandard veterinary drugs in Article 28 of the Act.
中文原文 動物用藥品管理法施行細則第5條
下列事項,各級主管機關得委任所屬機關或委託其他機關(構)、法人或團體辦理:
一、本法第十二條所定檢驗登記。
二、本法第十三條所定原登記事項之變更。
三、本法第十四條第一項所定動物用藥品許可證有效期間之展延。
四、本法第十八條所定抽樣及查驗。
五、本法第二十五條所定對動物用藥品製造業者之檢查。
六、本法第二十六條所定對動物用藥品製造業者、販賣業者、獸醫診療機構、禽畜與水產養殖業者、飼料製造業者或其他使用動物用藥品者之抽取樣品、稽查及抽樣檢查。
七、本法第二十八條所定對涉嫌之動物用偽藥、禁藥或劣藥之抽樣鑑定。

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