摘要
从兽药管理法规、兽药监督管理部门、新兽药的研制、兽药注册管理、兽药生产许可证和GMP、兽药经营许可与GSP、进口兽药管理和兽药分类管理等八个方面,分别列举和比较了中国与欧盟的法律法规、行政设置和管理规定。
Administrations of veterinary drugs in China and European Union were listed and compared including regulations, supervision , research and development of new veterinary drugs, registration and administration, the veterinary drug manufacturing licenses and GMP, veterinary drug distribution license and GSP, administration of importation of veterinary drugs and the administration system of classifying veterinary drugs.
出处
《中国兽药杂志》
2005年第3期1-5,共5页
Chinese Journal of Veterinary Drug
