Regulations for Medicament Contract Manufacture and Analysis Article 4
"Contract analysis," as used in these Regulations, means the contract of another firm or a relevant agency to carry out research and development in the technical aspects of medicinal products, control of production, quality control and stability testing for active pharmaceutical ingredients, semi-finished products, and end products.
中文原文 藥物委託製造及檢驗作業準則第4條
本準則所稱委託檢驗，係指將藥物技術層面之研究發展、製程中之管制作業及原物料、半製品或產品之品質管制與安定性試驗等項目，委託他廠或相關單位執行。