Veterinary Drugs Control Act Article 32-2
For categories of veterinary drugs which are promulgated by the central competent authority, veterinary drug manufacturers and importers shall compile and submit data (drug type, quantity produced or imported, quantity sold, and customer names) to special municipal or county (city) competent authorities for the record by the end of January and July each year, and also retain the data for three years.By the end of February and August each year, special municipal or county (city) competent authorities shall summarize and submit the data prescribed in the preceding Paragraph to the central competent authority.
中文原文 動物用藥品管理法第32-2條
動物用藥品製造業者及輸入業者,應於每年一月及七月底前,將前六個月製造或輸入,經中央主管機關公告之動物用藥品種類、數量、銷售量及銷售對象等資料,報請所在地直轄市或縣(市)主管機關備查,並將該資料保存三年。
直轄市或縣(市)主管機關應於每年二月底及八月底前,將前項資料彙報中央主管機關。
直轄市或縣(市)主管機關應於每年二月底及八月底前,將前項資料彙報中央主管機關。