1.
Photocopy of the Drug Import Registration Certificate (or the copy of Pharmaceutical Product Registration Certificate) and photocopy of the Drug Import Approval;
《进口药品注册证》（或者《医药产品注册证》）复印件、《进口药品批件》复印件；
2.
Preliminary analysis of Requirements for On-site Verification for Drug Registration;
浅析《药品注册现场核查管理规定》
3.
New Problems in FDA Problems in Drug Registration
FDA药品注册管理过程中的几个新问题
4.
An applicant forges or alters the relevant documents and vouchers; The Drug Import Registration Certificate (or the Pharmaceutical Registration Certificate) has been canceled;
伪造、变造有关文件和票据的；《进口药品注册证》（或者《医药产品注册证》）已被撤销的；
5.
Comparison and Analysis of Registration Authorisation Regulation of Veterinary Biological and Drug Product in U.S.A, EU and China;
国内外兽医药品注册管理规定的比较分析
6.
Solving Patent Problem in the Registration and Approval of Drugs;
药品注册审批工作中专利相关问题探讨
7.
Discussion on the Intellectual Property Protection in the Drug Registration Regulations
浅谈《药品注册管理办法》中的知识产权保护
8.
Comparative Study on Chinese and American Procedures of Drug Registration
中、美药品注册管理法规体系的比较研究
9.
Its tasks should relate in particular to establishing Community herbal monographs relevant for the registration as well as the authorisation of herbal medicinal products.
其任务主要是建立适用于草药品注册和授权的共同体草药专论。
10.
The New Amendment "Drugs Registered Management Measures" to Discuss the IV Clinical Trial Management;
从新修订《药品注册管理办法》谈IV期临床试验管理
11.
Relationship Among Drug Marketing Authorization,Manufacturing Authorization as Well as GMP Inspection
欧盟药品注册、企业生产许可证及GMP检查的相互关系
12.
Brief Introduction of Validation and Verification of Quality Specification of Import Drug in China
简述我国进口药品注册检验工作的历史、现状及展望
13.
Supplemental submission of application for investigational new drugs in China
创新性化学药品注册申请中补充资料相关问题的研究
14.
generic drug
不注册的药品,不受注册商标保护的药品
15.
Improve the Registration of Pharmaceutical Packaging Materials for the Safety and Effect of Medicines;
完善药包材注册管理 保障药品安全有效
16.
Connecting and Perfecting the Regulations on Medical Patent Investigation and Registration;
药品专利审查和新药注册制度的链接与完善
17.
Article41] With the exception of Chinese medicinal materials and Chinese medicines sliced and prepared for decoction, drugs must use a registered trademark and may not be sold on the market until examined and approved for registration.
第四十一条除中药材、药饮片外，药品必须使用注册商标；未经核准注册的，不得在市场销售。
18.
The registered trade mark of the products is... Brand.
产品注册商标为..