您要查找的是不是：
- Responsible for industry, science and technology, security, production quality and technical supervision, food and drug regulation, the information industry, etc. 负责工业、科技、安全生产、质量技术监督、食品药品监管、信息产业等方面的工作。
- And Chinese drug regulators have said that all producers of those ingredients are required to obtain certification by the State Food and Drug Administration. 中国的药品监管部门说，所有的那些配料生产者都要获得国家食品药品监督管理局的许可证。
- Nigerian food and drug regulators recently announced a death toll of 34 in an outbreak of fatalities among infants given a locally made baby formula tainted with a toxic thickening element. 日前，尼日利亚食品和药品监管部门发表声明，称该国生产的一种掺入有毒化学增稠剂的婴儿配方奶粉已造成34名婴儿死亡。
- Nigeria Food and Drug regulatory investigation found that the milk business from a business license and health did not permit the Department of Chemical Reagents dealer received a thickening agent. 尼日利亚食品和药品监管部门的调查人员发现，这家奶粉企业从一家没有营业执照和卫生许可的化学试剂经销商处获得了增稠剂。
- Exhibit A is the US Food and Drug Administration. 证据之一是美国食品和药物管理局。
- Food and Drug Administration, Conway said. 违反者将面临25美元至1000美元不等的罚款。
- More food and drugs have been hurried to the flooded areas. 已赶紧向水灾灾区送去了更多的食品和药品。
- State Food and Drug Administration issued SFDA Decree No. 国家食品药品监管局发布第十三号局令。
- This format is established by Jiangsu Food and Drug Administration. 本表由江苏省食品药品监督管理局制定。
- Secretary Leavitt is in China to discuss food and drug safety. 莱维特部长访问中国，讨论食品和药品安全问题。
- This statement has not been evaluated by the Food and Drug Administration. 这些声明未获得食品及药物管理局审核。
- food and drug regulation 食品药品监管
- These statements have not been evaluated by the Food and Drug Administration. 上述评价不是由fda做出的。
- The U.S. Food and Drug administration tries to regulate consumerism. 美国食品和医药管理局想规范消费者权益运动。
- The vaccine has been licensed by the US Food and Drug Administration. 一种被美国食品和药物管理局颁发执照的疫苗。
- File and send the register material to Food and Drug Administration. 产品注册资料报送国家食品药品监督管理部门；
- Regulation (QS) for Medical Devices: General regulation (21 CFR part 820) and that, through periodic (QS) inspections, the Food and Drug Administration (FDA) will verify such assumptions. 对医用装置的规定有：总规定（联邦法规全书第21章820条）和“食品和药物管理局”通过定期检查所确认的事项。
- Shall be separately formulated by the State Food and Drug Administration and the General Administration of Customs. 由国家食品药品监督管理局与海关总署另行制定。
- The U. S. Food and Drug administration classifies it as a food additive for tea. 美国食品和药物管理局把它归在茶的辅加食物一类。
- Last year, the U. S. Food and Drug Administration (FDA) approved a record of 21 new biotech products, BIO reports. 据生物技术公司报道，去年美国食品、药物管理局(fda)批准在案的有21项新的生物技术产品；
