开展药物临床试验应当经哪个部门审查同意？-法规政策咨询及电话投诉类法律援助-法律咨询免费平台-国际律师联盟

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问题	开展药物临床试验应当经哪个部门审查同意？
释义	法律分析：开展药物临床试验,应当经国务院药品监督管理部门依法批准。法律依据：《中华人民共和国疫苗管理法》第十六条开展疫苗临床试验，应当经国务院药品监督管理部门依法批准。疫苗临床试验应当由符合国务院药品监督管理部门和国务院卫生健康主管部门规定条件的三级医疗机构或者省级以上疾病预防控制机构实施或者组织实施。国家鼓励符合条件的医疗机构、疾病预防控制机构等依法开展疫苗临床试验。
随便看	质量成本计算的方法什么是工程质量生产日期和保质期计算器质量事故的划分工程质量的概念是什么意思什么是一般质量事故工程质量的定义是指什么工程质量的定义是指什么工程质量的定义什么是质量管理体系？什么是工程质量？质量事故的定义及划分什么是一般质量事故工程质量定义有哪些工程质量的概念和内容是什么？什么是质量管理体系？工程质量概念是什么内容再审申请书的答辩意见怎么写？申请复议—司考真题答案解析反诉—司考真题答案解析二手房过户问题与购买权探讨再审—司考真题答案解析二审被上诉人答辩状格式范文申诉的办理—司考真题答案解析二手房买卖合同过户纠纷 administrative department in charge of the auto industry administrative department in charge of the chemical industry administrative department in charge of the coal industry administrative department in charge of the electronics industry administrative department in charge of the iron and steel industry administrative department in charge of the light industry administrative department in charge of the manufacturing industry administrative department in charge of the metallurgical industry administrative department in charge of the production and operation of pharmaceuticals administrative department in charge of the registration of companies administrative department in charge of the shipbuilding industry administrative department in charge of the transport service administrative department in charge of tourist industry administrative department in charge of urban planning administrative department in charge of water conservancy administrative department of public security administrative department under reconsideration administrative departmet for archives administrative deposition administrative detention administrative determination administrative directive administrative disciplinary measures administrative discretion administrative disposal

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