节点文献
仿制药注册申报资料整理要求综述
Review on sorting requirements of the generic drug registration application
【摘要】 本文根据国家食品药品监督管理局对仿制药研究的法规和要求,整理了仿制药注册申报形式要求和注意事项,以期对仿制药的注册申报有一定的指导意义。
【Abstract】 Base on the the regulations and requirements for the generic drug by the State Food and Drug Administration,this article sorted the requirements and considerations for generic drug registration application,with a view to have certain significances for the registration of generic drug.
- 【文献出处】 齐鲁药事 ,Qilu Pharmaceutical Affairs , 编辑部邮箱 ,2012年02期
- 【分类号】R95;F203
- 【被引频次】1
- 【下载频次】548