1.
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
2.
Veterinary Clinical Drug Development and Registration-Understanding the Dynamics of the Healthcare Transaction to Achieve Successful Economic Outcomes
兽医临床药品的研发与注册——了解兽医医疗保健的动态以获得最大的经济效益
3.
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；
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.
generic drug
不注册的药品,不受注册商标保护的药品
6.
Class10 Surgical, medical, dental and veterinary apparatus and instruments, artificial limbs, eyes and teeth; orthopaedic articles; suture materials.
商标注册类别10外科、学、科和兽医用仪器及器械，假肢、眼和假牙；矫形用品；缝合用材料。
7.
The Manual also contains the protocols for the production and the control of biologics for veterinary use.
手册还包含有兽医用生物制品生产和控制协议。
8.
Requirement and Suggestion on Re-registration of Imported Veterinary Biologics
进口兽用生物制品再注册申报的要求及建议
9.
Registration Committee [Chinese Medicine Council of Hong Kong]
注册事务小组〔香港中医药管理委员会〕
10.
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。
11.
The term of validity for the registration certificate of medical devices is four years.
医疗器械产品注册证书有效期四年。
12.
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》
13.
New Problems in FDA Problems in Drug Registration
FDA药品注册管理过程中的几个新问题
14.
Comparison of Administration of Veterinary Biological Product Registration Between China and U.S.A, EU;
中国与美国及欧盟兽用生物制品注册管理的比较分析
15.
register of medical laboratory technologists
医务化验师注册名册
16.
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
17.
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
18.
Feasibility for Establishing East Asia Traditional Medicine Conference On Harmonization
建立东亚传统医药注册协调会的可行性分析