Regulatory science accelerates the development of biotechnology drugs and vaccines by NIFDC

被引：1
作者：
Liang, Zhenglun [1 ]
Mao, Qunying [1 ]
Wang, Yiping [1 ]
Li, Changgui [1 ]
Gao, Kai [1 ]
Wang, Junzhi [1 ]
机构：
[1] Natl Inst Food & Drug Control, Beijing 100050, Peoples R China
来源：
EMERGING MICROBES & INFECTIONS | 2014年 / 3卷
关键词：
biotechnology drug; quality control; vaccine; ENTEROVIRUS; 71; VACCINE; PANDEMIC INFLUENZA VACCINE; NEUTRALIZING ANTIBODY; UNIVERSAL ANTIBODIES; DOUBLE-BLIND; SAFETY; IMMUNOGENICITY; EFFICACY; STANDARD; SUBTYPES;
D O I：
10.1038/emi.2014.66
中图分类号：
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号：
100102 ;
摘要：
The Chinese National Institutes for Food and Drug Control (NIFDC) is the national laboratory responsible for the quality control of pharmaceutical products. In recent years, to ensure the quality of biological products and improve the research and development (R& D) of new biological drugs and vaccines, NIFDC conducted a series of regulatory science studies on key technologies for quality control and evaluation, and established a quality control and evaluation platform for biological drugs and vaccines. These studies accelerated the R&D of the biological drugs and vaccines in China and assured their safety and efficacy. In this paper, NIFDC's duties and achievements in the biological drug and vaccine field are summarized.
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页数：4
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