Quality management system assessment report issued by SFDA;
质量管理体系考核报告；
The process to apply for the SFDA manufacturing license is in progress.
SFDA生产许可证的申请正在进行中。
All her products are GMP certified by the State Food and Drug Administration (SFDA).
所有产品均通过国家食品药品监督管理局GMP认证。
Bottled water and Tap water Regulation sFDA and state bottled water programs are seriously underfunded.
美国食品药品局对瓶装水的管理缺乏资金。
But the Chinese SFDA will not issue a new drug license for a compound that we already have a patent for.
但中国国家食品药品监督管理局不会对我们已经拥有专利的药品发放新药许可。
Article 21 SFDA shall determine whether to approve the application according to the comprehensive evaluation opinion brought forward by CDE.
第二十一条国家食品药品监督管理局依据药品审评中心的综合意见，作出审批决定。
But as the SFDA tries to raise standards for its drug-approval processes, some are worried that smaller companies will not be able to survive.
但当SFDA试着要将其药品认证程序标准化时，一些人却担心以些小一点的公司将无法生存。
Based on clients' requirement, the company can meet relevant GMP of SFDA, FDA, EMEA or WHO, and provide relevant validation support documents.
公司能根据客户要求，分别符合SFDA、FDA、EMEA或WHO等相关的GMP要求进行设计和制作，并提供相关的验证支持文件。
Thee SFDA cautioned consumers, especially the younger generations, against health care foodstuff, for these sometimes contain materials unfit for adolescents.
国家食药监局提醒消费者，特别是青少年，要谨慎对待保健食品，有些保健食品原料不太适合年轻人使用。 。
Article 3 the State Food and Drug administration (SFDA) shall be in charge of the nationwide supervision, administration and coordination of accredited supervisors.
第三条国家食品药品监督管理局负责全国派驻监督员的监督管理及协调工作。
Clinical research found little evidence proving that Duxil effectively improves cognitive ability in patients suffering vascular cognitive impairment, the SFDA said.
国家药监局称，临床试验结果不支持服用“都可喜”能够有效提高血管性认知障碍患者的认知功能。
The new SFDA regulation: Requirements for on-site verification for Drug Registration was analyzed and the impact to present work of on-site verification was concluded.
分析了《药品注册现场核查管理规定》的出台对药品注册现场核查工作可能产生的影响，对《规定》中的一些内容进行了探讨。
The thesis first analyzes a case how SFDA in China doling with the affair that medical institution sold counterfeit drugs, and the analysis lead to the study of the whole administration system.
文章首先采用现代法学理论的成因分析方法对基层医疗机构销售假、劣药品行为进行分析，研究其违法动机、违法方式和违法目的。
The thesis first analyzes a case how SFDA in China doling with the affair that medical institution sold counterfeit drugs, and the analysis lead to the study of the whole administration system.
文章首先采用现代法学理论的成因分析方法对基层医疗机构销售假、劣药品行为进行分析，研究其违法动机、违法方式和违法目的。
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