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国家药品监督管理局药品审评中心 国家药品监督管理局药品审评中心 CENTER FOR DRUG EVALUATION, NMPA 网站地图 联系我们 CDE邮箱 搜索
California Department of Education CDE has launched a toolkit of family-facing posters and notecards that communicate assurance of all schools’ obligation to provide every child with access to education and a safe learning environment, regardless of immigration status
医药注册小百科｜CDE详解 🔍CDE，全称Center for Drug Evaluation，即药品审评中心。 它是中国国家药品监督管理局的直属单位，负责药物临床试验、上市申请等的受理和技术审评，以及拟定指导原则等其他技术工作。
药品审评中心 药品审评中心（CENTER FOR DRUG EVALUATION,CDE）是国家药品监督管理局药品注册技术审评机构，为药品注册提供技术支持。 按照国家药品监督管理局颁布的药品注册管理有关规章，负责组织对药品注册申请进行技术审评。
Center for Drug Evaluation of NMPA Main responsibilities (1) Be responsible for the acceptance and technical review of applications for drug clinical trials and drug marketing authorization (2) Be responsible for the technical review on the consistency evaluation on the quality and efficacy of generic drugs (3) Undertake the technical review of drugs involved in emerging medical products such as regenerative medicine and