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Clinical trials

Clinical trials are sets of tests performed for medical research and drug development which is used to extract safety and efficacy data.

临床试验的贡献者

Clinical trials

协议

制药; 临床试验

A study plan on which all clinical trials are based. The plan is carefully designed to safeguard the health of the participants as well as answer specific research questions. A protocol describes ...

美国食品和药物管理局

制药; 临床试验

Food and Drug Administration. The U.S. Department of Health and Human Services agency responsible for ensuring the safety and effectiveness of all drugs, biologics, vaccines, and medical devices, ...

不良反应

制药; 临床试验

(不良事件)。药物的行政当局所引起的副作用。发病可能突然或时间 (见副作用) 的发展。

批准的药品

制药; 临床试验

在美国,食品和药物管理局 (FDA) 之前必须批准一种物质作为一种药物可以销售。审批过程涉及几个步骤包括临床前的实验室和动物研究中,为安全和疗效,通过药物的制造商、 FDA 审查的应用程序和 FDA 批准/拒绝应用程序的新药物申请的临床试验。 ...

制药; 临床试验

Any of the treatment groups in a randomized trial. Most randomized trials have two "arms," but some have three "arms," or even more.

临床的

制药; 临床试验

与有关的或基础上的观察和处理参与者,它有别于理论的或基本的科学。

基于社区的临床试验(CBCT)

制药; 临床试验

主要通过初级保健医师而不是学术研究设施进行的一项临床试验。

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