Guidelines of Good Manufacture Practice (GMP)for Veterinary Drugs Manufacturers Article 8
The Manufacturer shall order the written detailed operating procedures concerning the quality standards of raw materials, product containers or seals and the check on delivery, labeling, storage, treatment, sampling,inspection and examination concerned.The containers packaging starting materials and product containers or seals shall be marked batch by batch with clear codes and the statuses of under test, acceptance, rejection or quarantine required along with the treatment records of the batches of objects.
中文原文 動物用藥品優良製造準則第8條
藥廠應以書面詳訂對原料、產品容器或封蓋之品質規格及其驗收、標識、儲存、處理、取樣、檢驗及審核等作業程序。
盛裝原料、產品容器或封蓋之容器，應逐批標示明確之代號及待驗、准用、拒用或須隔離之狀況，並應記載於各批物品之處置紀錄。
盛裝原料、產品容器或封蓋之容器，應逐批標示明確之代號及待驗、准用、拒用或須隔離之狀況，並應記載於各批物品之處置紀錄。