Veterinary Drugs Control Act Article 18
After veterinary biologics are produced or have cleared the customs with all tariffs paid, the manufacturer or importer shall apply to special municipal or county (city) competent authorities for batch-by-batch sample testing; such a drug may not be sold until it has passed sample testing and inspection and is secured with the seal of approval by personnel dispatched from the relevant competent authority.Regulations governing the inspection in the preceding Paragraph are to be prescribed by the central competent authority.
中文原文 動物用藥品管理法第18條
動物用生物藥品，於製成或輸入報關完稅後，製造業者或輸入業者應逐批向直轄市或縣（市）主管機關申請抽樣檢驗，經該管主管機關派員抽取樣品，查驗合格並封緘後，始得出售。
前項查驗辦法，由中央主管機關定之。
前項查驗辦法，由中央主管機關定之。