Pharmaceutical Affairs Act Article 43
Application forms to be used for applying for registration and market approval of manufacture or import of medicaments, quantities of samples and relevant information required and registration fees shall be established by the central competent health authority.
中文原文 藥事法第43條
製造、輸入藥物之查驗登記申請書及輸出藥物之申請書，其格式、樣品份數、有關資料或證書費、查驗費之金額，由中央衛生主管機關定之。