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1)  new drug registration
新药注册
1.
Results and Conclusion Through the American experience,active steps to amend the"Drug Administration Law,"to improve the level of R & D of new drugs and new drug registration capability.
目的促进《药品管理法》修订,提高我国新药研究能力与新药注册审评水平。
2)  the new drug application
新药注册申请
3)  drug registration
药品注册
1.
Investigation on mode of on-site examination in drug registration;
药品注册现场核查模式探讨
2.
Stability studies in drug registration
药品注册中的稳定性研究
3.
The system of drug registration and management in China has gone through the three stages of initiation, formation and completion since the founding of new China, and since 1985 when the Law of Drug Management began to be enforced in particular, the reform of examination and evaluation mechanisms of drugs has ever gone deeply.
中国的药品注册管理制度自新中国成立以来,经历了初始、形成和完善三个阶段。
4)  Freshmen Register
新生注册
1.
According to the features and demands of freshmen register work in colleges, my thesis has developed, designed and realized the College Freshmen Register System which possesses the three-tier C/S system by applying UML modeling techniques, Jaguar component techniques and data mining techniques.
本文针对高校新生注册工作的特点和需要,应用UML建模技术、Jaguar组件技术和数据挖掘技术开发并设计实现了具有三层C/S体系结构的高等院校新生注册管理系统,并在系统开发过程中对相关技术进行了研究实践。
5)  drug re-registration
药品再注册
6)  imported drugs registration
进口药注册
1.
Clinical research strategies for imported drugs registration
本文从进口药注册临床试验的争论入手,回答是否需要开展注册临床试验和需要开展什么样的注册试验。
补充资料:新药
1.指新创制的药物。 2.指西药。
说明:补充资料仅用于学习参考,请勿用于其它任何用途。
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