Pharmaceutical Good Manufacturing Practice Regulations Article 132
Manufacturers shall carry out final inspection and testing and prepare records in accordance with the quality plan or documented procedures to ensure conformance of the finished product to the specified requirements.
中文原文 藥物優良製造準則第132條
製造業者應依品質計畫或書面程序執行最終檢驗與測試並作紀錄，以確認最終產品符合規定要求。