sfda
- 网络国家食品药品监督管理局(State Food and Drug Administration)；国家药监局；中国食品药品监督管理局
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国家食品药品监督管理局(State Food and Drug Administration)
国家食品药品监督管理局（sfda）前局长郑小臾说过，所有的增高药都是假的，SFDA根本就没批准过任何增高产品，2005年8 …
国家药监局
除经国家药监局(SFDA)批准的药品委托生产和异地加工外，对生产同一药品的不同企业发给不同的药品批准文号。药品生产企 …
中国食品药品监督管理局
搜索中国食品药品监督管理局（SFDA）里面可以搜到生产许可证！|评论 "施慧达"是药品的商品名，本药品的通用名叫“苯磺酸 …
国家食品药品监管局
在国家食品药品监管局(SFDA)的药品数据库中，国际戒烟药目前常用的品种中，包括尼古丁替代疗法的药物，国内企业只有一 …
中国药监局
中国药监局(SFDA)API的GMP检查及欧美出口确认程序Panel Discussion: International Regulatory Collaboration and Challenge…
1
Hualan is the largest producer of vaccine in Asia with a state of the art facility that operates according to sFDA GMP and EU guidelines.
华兰是与最先进的设施，国家在亚洲最大的疫苗生产商的操作根据国家药监局GMP和欧盟的指导方针。
2
SFDA will be on the site of the drugs production enterprise " GMP inspection certificate" continue to be publicity.
SFDA将在网站上对药品生产企业《药品GMP证书》延续情况予以公示。
3
The scandal centres around Zheng Xiaoyu, who was the head of the State Food and Drug Administration (SFDA) from 1998 until June 2005.
丑闻的中心是郑晓臾，1998年-2005年六月间任国家食品药品管理局（SFDA）的局长。
4
The SFDA may designate an institute for drug control to make a selective inspection over the drugs for clinical trial use.
国家食品药品监督管理局可以指定药品检验所对临床试验用的药物进行抽查检验。
5
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。
6
Innovative drug bulletin Providing information about SFDA new drug market approval bulletin and FDA new drug approval bulletin.
科技技术转让信息；J新药公告国家药监局发布的新药公告、FDA发布新药批准公告；
7
Make and update related SOP to comply with corporate and SFDA requirement; Prepare facility related validation report if needed.
制定和更新相关SOP以符合总部及药监局的相关要求；根据项目需要准备设施的验证文件。
8
Maintain good relationship with related government officers, incl. customs, SFDA, CIQ etc.
与相关政府部门保持良好的关系，包括海关、药检、商检等。
9
Shao Mingli, head of the SFDA, said that the WHO approval showed that China had improved vaccine regulation and could guarantee quality.
SFDA局长邵明立说，世界卫生组织的批准表明中国已经改进了疫苗监管而且可以确保质量。
10
Organize and prepare all the documents and materials about registration in SFDA.
协助整理和准备申报注册的全部文件、材料；
11
The June 2nd tenth world pharmaceutical raw materials of Chinese exhibition, SFDA officials also revealed similar information.
6月2日第十届世界制药原料中国展上，国度药监局官员也走漏出类似的信息。
12
Review, revise clinical study report, ensure it meet the registration requirement of SFDA.
审核修改临床研究协调员撰写的临床研究总结报告，并符合国家药品注册的要求；
13
Participate in registration of import and local manufacturing medical device in SFDA.
参与进口和国产医疗器械的注册。
14
Objective: Study pharmaceutical technology of total Ginseng saponin for injection according to SFDA new registration.
目的：按国家新的中药注射剂注册要求制备注射用人参总皂苷。
15
The State Food and Drug Administration (SFDA) Wednesday blacklisted 25 websites for selling fake medicines.
11日，国家食品药品监督管理局发布了2009年第1期互联网购药安全警示公告，25家网站因销售假药被曝光。
16
Send the sample to Medical Devices Testing Center approved by SFDA to test, and obtain the test report.
代理产品（检测样品）在SFDA认可的检测中心检测、领取检测报告；
17
The SFDA pledged to publicize information on dietary supplements with health risks and stop its distribution.
管理局保证公开那些对健康有害的健康保健品的信息，并停止其供应。
18
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。
19
Set up test requirement for testing outside China, for imported products. (According to SFDA).
（根据SFDA）建立进口产品在中国之外测试的测试要求。
20
No major adverse reactions were detected in clinical trials, said Li Guoqing, who heads the SFDA's Drug ation Center.
临床试验中并没有发现疫苗有重大的不良反应。
21
"You need another body to watch the SFDA, " says Liu.
“你需要一个人来看着SFDA”，刘说。
22
China has 36 sites manufacturing 49 vaccines for 27 diseases with an annual capacity of nearly one billion doses, according to the SFDA.
SFDA说，中国有生产27种疾病的49种疫苗的36个厂家，年生产能力接近10亿份。
23
Preparing, submitting and maintenance of product certificates from SFDA, CMC etc for products sold in China.
准备，递送和维护SFDA，CMC等发放的在中国销售的产品证书。
24
the total content of effective part in the extracts is over 50%, which is accord with relevant regulations of SFDA.
其提取物有效成分的总含量达到50%以上，符合国家食品药品监督管理局的相关规定。
25
There are 27 biotech drugs approved by SFDA in China.
中国批准了27种生物技术药物。
26
SFDA Issues Notice Distinguishing Between a Medical and a Pharmaceutical Product for Registration Purposes
国家食品药品监管局明确药品和医疗器械相结合产品注册管理有关问题
27
SFDA Temporarily Adjusts the Methods of Submitting and Reviewing Registration Applications
药监局临时调整药品注册申报受理方式
28
SFDA Decides to Set Up a Think Tank for Health Foods
国家食品药品监管局决定建立保健食品审评专家库
29
Coordinate the relationship with other departments, keep good contact with customers, SFDA and CMDE;
协调技术部与其他部门的关系，与客户、SFDA以及CMDE保持联系；
30
Requirements of management management SFDA CCD
管理要求