Guidelines of Good Manufacture Practice (GMP)for Veterinary Drugs Manufacturers Article 25
There shall be individual storage and proper marking for the labels and other package materials in accordance with the product categories, strength / contents or dosage forms. It is prohibited to enter the aforementioned storage area without the agreement of the competent personnel.The packaging and labeling materials inapplicable to use or with the rejection shall be returned or destroyed. The issuance and utility and the returned quantity of the labeling materials shall be identical.The labeling materials printed with the batch number shall be destroyed immediately if there is any residual; the labeling materials with no batch number shall be properly examined and stored to avoid mix-ups.
中文原文 動物用藥品優良製造準則第25條
標籤及其他標示材料,應依產品之種類、含量或劑型,分別儲存,並予適當之標識;其儲存區域,非經權責人員同意,不得進入。
不堪使用或拒用之包裝材料及標示材料,應予退貨或銷燬,標示材料之發放與使用及退回數量,應相符合。
印有批號之標示材料,如有剩餘應即予銷燬,其他未印者,應予適當鑑識、儲存,避免混雜。
不堪使用或拒用之包裝材料及標示材料,應予退貨或銷燬,標示材料之發放與使用及退回數量,應相符合。
印有批號之標示材料,如有剩餘應即予銷燬,其他未印者,應予適當鑑識、儲存,避免混雜。