常用药品监管英语与缩略语.doc

常用药品监管英语与缩略语
监管英语
1.《中华人民共和国药品管理法》
Drug Control Law of the People's Republic of China

control over drug manufacturers

control over drug distributors

control over medicines in medical institutions

control over drugs

control over drug packaging

control over drug price and advertisement

inspection of drugs

legal liabilities

labels or marks of the drugs

counterfeit drugs

inferior drugs

drug quality control laboratory

drug manufacturers

drug distributors

medical institutions

drug regulatory agency

drug approval documents

administrative sanctions

criminal liabilities

Good Manufacturing Practice for Pharmaceutical Products (GMP)

Good Supply Practice for Pharmaceutical Products (GSP)

Drug Manufacturing Certificate

Drug Supply Certificate

Pharmaceutical Preparation Certificate for Medical Institution

Import Drug License

clinical trial

New Drug Certificate

Drug Approval Number
、生产、经营、使用和监督管理的单位或者个人,必须遵守《中华人民共和国药品管理法》
All institutions or individuals engaged in research, production, distribution, use, and administration and supervision of drugs in the People's Republic of China shall abide by drug control law of the people's republic of China.
。
The drug regulatory agency of the State Council shall be responsible for drug administration and supervision nationwide.
、自治区、直辖市人民政府药品监督管理部门负责本行政区域内的药品监督管理工作。
The drug regulatory agencies of the governments of provinces, autonomous regions, and municipalities directly under the Central Government shall be responsible for drug regulation in their administrative areas.
,承担依法实施药品审批和药品质量监督检查所需的药品检验工作。
The drug quality control