Guidelines of Good Manufacture Practice (GMP)for Veterinary Drugs Manufacturers Article 24

There shall be written control operating procedures for the check on delivery, labeling, storage, management, sampling and test of packaging and labeling materials which shall be complied with.The representative sample shall be inspected through batch-by- batch sampling at the check on delivery of or prior to the employment of the labeling or packaging materials. The result shall be recorded and reserved. Those with the conformity to the existing specifications may be granted the acceptance whereas those with the inconformity may be granted the rejection.
中文原文 動物用藥品優良製造準則第24條
包裝材料及標示材料之驗收、標識、儲存、管理、取樣及檢驗等項目,應訂立書面管制作業程序,並遵行之。
標示材料或包裝材料於驗收或使用前,應逐批抽取具代表性之樣品予以檢驗,記錄其結果,並保存之。
檢驗結果符合既定規格者,始予准用;不符者拒用之。

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