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关注：1
2013-05-23 12:21
求翻译：了解新药开发的基本原则及药品相关的法律法规指导原则（ICH、USP、Chp、GMP、药品注册管理办法），能撰写药品申报资料。是什么意思？ 待解决
 悬赏分：1
- 离问题结束还有
了解新药开发的基本原则及药品相关的法律法规指导原则（ICH、USP、Chp、GMP、药品注册管理办法），能撰写药品申报资料。
问题补充： |
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2013-05-23 12:21:38
正在翻译，请等待...
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2013-05-23 12:23:18
Understanding the basic principles of development new drugs and drug related laws and regulations guiding principles (ICH USP , , , Chp GMP), drug registration management approach to writing, drug information returns.
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2013-05-23 12:24:58
Understood the new medicine development the basic principle and the drugs correlation legal laws and regulations guiding principle (ICH, USP, Chp, GMP, drugs registration policing method), can compose the drugs declaration material.
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2013-05-23 12:26:38
Understand the basic principles of the development of new drugs and drug-related laws and regulations guiding principles (ICH, USP and Chp, GMP, medicines registration management approaches), to written drug information.
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2013-05-23 12:28:18
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