中华人民共和国药品管理法 Law of the People's Republic of China on the Administration of Pharmaceuticals
食品药品管理法修正案 FDAAA
药品管理法律法规 GMP & cGMP
动物用药品管理法 Veterinary Drugs Control Act
药品注册管理办法 provisions for drug registration
精神药品管理办法 measures for the control of psychotropic drugs
药品和化妆品管理法 FD&C Act
药品价格管理办法 Drug Price Control Measures
目的:完善《药品管理法》修订,以加强医疗机构药品监管。
Objective:The consummation《Pharmaceutical Administration Law》revises, strengthens the Medical institutions drugs supervision.
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。
Objective To perfect drug administration law of the People's Republic of China by establishing the adverse drug reaction (ADR) relief system.
随着新的《药品管理法》的实施,各类药品都将有一个效期管理的问题存在。
With the implementation of the new Law of Drug Control, the problem of expiry date has come to draw public attention.
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