2010-01-012024-05-15https://scholars.lib.ntu.edu.tw/handle/123456789/663273摘要：研析先進國家動物和我國人用藥品之管理規範，針對我國動物動物用藥品檢驗登記之審查標準，研提建議草案，籌組成立動物用藥品專家委員會，並對部分受關注之動物用藥品項目及其新知，進行科學評析和檢討，提出刪減品項供主管當局參考，以健全國內管理動物用藥品檢驗登記的相關規範，促使國內法規的完備以及與國際接軌。<br> Abstract: Collect, study and compare domestic and internatinoal regulations for the registration of veterinary medicinal products. Establish an expert committee on veterinary drug regulations to discuss and review the proposed draft guidelines for the requirements of the registration of veterinary medicinal products. The draft guidelines will be submitted upon condition that the committee reaches consensus on the proposed drafts. Study and analyze specific items of veterinary drugs that are under evaluation for safety and efficacy issues. A suggestion for certain veterinary medicinal products to be withdrawn from the current market will be proposed based on the results of regulatory and scientific analysis on currently available data. The overall objective is to strengthen the demostic regulatory system for the registration and monitoring of vetrinary medicinal products, which will meet the global standard and requirement in the long run.動物用藥品檢驗登記法規研究veterinary drugregistrationregulatory study