1) the amendment of the Pharmaceutical Administration Law
药品管理法修改
2) 《Pharmaceutical Administration Law》revises
《药品管理法》修订
1.
Objective:The consummation《Pharmaceutical Administration Law》revises,strengthens the Medical institutions drugs supervision.
目的:完善《药品管理法》修订,以加强医疗机构药品监管。
3) Drug Administration Law
药品管理法
1.
Comparison between US FDCA and Drug Administration Law of PRC;
美国FDCA与我国药品管理法
2.
Suggestion on the Revising of Drug Administration Law;
关于修改《药品管理法》的思考
3.
“Drug Administration Law of PRC” and Protection for Human Rights;
《药品管理法》与人权保护
4) The Drug Administration Law of China
药品管理法
1.
Analysis on Definition of Counterfeit Drugs in the Drug Administration Law of China
现行《药品管理法》中假药定义剖析
2.
Results:The Drug Administration Law of China needs to be improved in aspects of the definition of new drug,the standards to divide the counterfeit drug and the adulterated drug,and the confirmation of the responsibility for the drug damage compensation.
目的:探讨我国药品安全监管中存在的法律问题,为《药品管理法》的再修订提供参考。
5) modification of"Land Administration Law"
土地管理法修改
6) drug management
药品管理
1.
The paper introduced the computer management in Hospital Drugs to make standardization of medicines management,to strengthen drug management,to block assets lost and reduce the phenomenon of stealing and missing charge.
通过对医院药品实现计算机管理,使药品管理规范化,加强药品管理,堵住资产流失,减少乃至杜绝偷、漏费现象。
2.
Objective To understand drug management of inpatient medical wards in our hospital and insure the safety and efficiency of drug using.
目的了解我院病区药柜的药品管理情况,确保临床用药安全有效。
补充资料：药品
1.药物和化学试剂的总称。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条