... 药品负责期 allotted date of drug quality ensuring by manufacturer 药品管理法 drug administration law 药品批号 drug batch number ...
基于1个网页-相关网页
Objective To perfect drug administration law of the People's Republic of China by establishing the adverse drug reaction (ADR) relief system.
目的建立我国药品不良反应救济制度,使《药品管理法》更加完善。
Results and Conclusions The definition of counterfeit drugs in the Drug Administration Law of China is not applicable to various types of drugs. The definition need to be amended.
结果与结论现行《药品管理法》中的假药定义不能有效地适用于各种类型药品的假药判定,需要进行改进。
The new law gives the US Food and Drug Administration the power to strictly limit the manufacturing and marketing of tobacco products.
新的法律给美国的食品和药品的生产,烟草的生产市场带来很大的限制。
应用推荐