1.
Reform Fooddrug Supervision System Promote Public Food Medicine Safety;
改革食品药品监管体制 保障公众饮食用药安全
2.
Appear afore-mentioned problems, can superintend a branch to complain to food medicines and chemical reagents.
出现上述问题，可向食品药品监管部门投诉。
3.
Food & Drug Surveillance Performance Appraisal and Application Research;
食品药品监管系统绩效评估方法与应用研究
4.
An analysis on enforcement equipment resource of food and drug administrations in China
我国食品药品监管机构执法装备资源状况分析
5.
Order of the State Food and Drug Administration
国家食品药品监督管理局令
6.
State Food and Drug Administration
国家食品和药品监督管理局
7.
and shall simultaneously submit it to both the State Food and Drug Administration and the National Institute for the Control of Pharmaceutical and Biological Products.
同时报送国家食品药品监督管理局和中国药品生物制品检定所。
8.
Decree No. 6 of the State Food and Drug Administration of the People's Republic of China, Promulgating the Measures for the Administration of Business Licenses of Drugs
国家食品药品监督管理局令第6号,发布《药品经营许可证管理办法》
9.
Overview on Development of State Food and Drug Supervision Informatization in 2003-2004
2003-2004年国家食品药品监督管理信息化发展概况
10.
This format is established by Jiangsu Food and Drug Administration.
2本表由江苏省食品药品监督管理局制定。
11.
Study & Strategetic Countermeasure on Current State of Manpower Resources of State Food and Drug Administration;
全国食品药品监督管理系统人力资源现状研究
12.
The Design and Implementation of the Management System of Jinan Food and Drug Administration
济南市食品药品监督管理系统的设计与实现
13.
U.S. Food and Drug Administration(FDA)
美国食品药品管理局
14.
The Food and Drug Administration, however,
不过，食品和药品管理局，
15.
The biological products as prescribed by the State Food and Drug Administration; The drugs sold within China for the first time; Other drugs as prescribed by the State Council
国家食品药品监督管理局规定的生物制品；首次在中国境内销售的药品；国务院规定的其他药品。
16.
In terms of the biological products within the range of examination, approval and issuance specified by the State Food and Drug Administration,
国家食品药品监督管理局规定批签发的生物制品，
17.
For a biological product within the range of examination, approval and issuance specified by the State Food and Drug Administration
国家食品药品监督管理局规定批签发的生物制品
18.
The packages and labels of the drugs that have arrived at the port are inconsistent with the requirements of the State Food and Drug Administration;
到岸品种的包装、标签与国家食品药品监督管理局的规定不符的；