1.
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
2.
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
3.
Consideration for the guideline to the generic drugs development and review to meet the revised Drug Registration Regulation;
新版《药品注册管理办法》的实施对仿制药研发与技术评价要求的初步考虑
4.
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
5.
With the Drug Supply Certificate, the wholesaler and the retailer shall be registered with the administrative agency for industry and commerce.
药品批发、售企业凭《药品经营许可证》到工商行政管理部门办理登记注册。
6.
With the Drug Supply Certificate , the wholesaler and the retailer shall be registered with the administrative agency for industry and commerce.
药品批发、零售企业凭《药品经营许可证》到工商行政管理部门办理登记注册。
7.
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》
8.
New Problems in FDA Problems in Drug Registration
FDA药品注册管理过程中的几个新问题
9.
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
10.
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
11.
The Regulation on Medicine Information Service via Internet
互联网药品信息服务管理办法
12.
Decree No. 6 of the State Food and Drug Administration of the People's Republic of China, Promulgating the Measures for the Administration of Business Licenses of Drugs
国家食品药品监督管理局令第6号,发布《药品经营许可证管理办法》
13.
Notification of the State Food and Drug Administration of the People's Republic of China, on Implementing the Record Checking Procedures in the re-registering application for Imported Drugs
国家食品药品监督管理局关于进口药品再注册申请实行核档程序的通告
14.
Registration Committee [Chinese Medicine Council of Hong Kong]
注册事务小组〔香港中医药管理委员会〕
15.
In case a new product has going through the above procedures and is found compliance with requirements, apply to the drug administration department for new product registration.
对完成上述步骤,符合条件的医疗器械产品,向药品监督管理部门申请产品注册。
16.
generic drug
不注册的药品,不受注册商标保护的药品
17.
Shallowly Discussion about Slight Defect of the Individual Provision on "Drugs Circulation Supervision and Management Method";
浅谈《药品流通监督管理办法》个别条款的瑕疵
18.
Decree No.6 of the State Administration for Industry and Commerce of the People's Republic of China, Promulgating Measures for Registration and Administration of Collective Marks and Certification Marks
中华人民共和国国家工商行政管理总局令第6号,发布《集体商标、证明商标注册和管理办法》