1.
Medical device manufacturers (shall be designated as manufacturers hereinafter) shall not only conform to the Pharmaceutical Affairs Law, But their quality systems shall also follow this practice for the implementation.
医疗器材制造工厂(以下简称制造业者)除应符合药事法规定外,其质量制度应依本规范实施。
2.
The Japanese Pharmacopoeia (JP) was designated as the official Japanese drug standard by The Pharmaceutical Administration Law of Japan.
药局方>>(JP)是日本《药事法》中规定的日本药品的法定标准。
3.
This practice has been established Based on Article 57 of the Pharmaceutical Affairs Law.
本规范依药事法第五十七条之规定建立。
4.
Discussion of "The Chinese Medicine Cocktail" Innovative Teaching Mode in Vocational Colleges--In the Case of Pharmaceutical Administration and Regulation Course
高职院校“中药鸡尾酒”式创新教学模式探讨——以《药事管理与法规》课程为例
5.
Unify the Packing of Chinese Herbal Pieces for Development of Traditional Chinese Medicine
规范中药饮片包装弘扬祖国中医药事业
6.
act in conformity with the rules, law, etc
依照规定、 法律等行事
7.
Rome Statute of the International Criminal Court
国际刑事法院罗马规约
8.
To order the use of(a medicine or other treatment).
规定嘱咐（某药或其它疗法）的用法
9.
(6) To exercise other powers and functions as prescribed in the rules of procedure of the Legislative Council.
（六）立法会议事规则所规定的其他职权。
10.
The military statutes and regulations are implemented within the armed forces.
军事法规、军事规章在武装力量内部实施；
11.
The International Law Problem on Restricted Use of Cluster Munitions;
限制使用集束弹药的国际法规制问题
12.
The Admiralty court was declared by statute to be a sovereign court.
法律规定海事法庭是最高管辖法庭。
13.
Commissioning Manufacture of Overseas Drugs in China in view of the Amendment of the Pharmaceutical Affairs Law in Japan;
从日本药事法的修订谈我国境外药品委托生产
14.
Qi-Er-Yao,Herba Houttuyniae and Xinfu:legal thinking on drug injury events;
齐二药、鱼腥草与欣弗:药品安全事件的法律思考
15.
Supervision System on Drug Manufacturing in China;
从“齐二药”事件谈我国药品监管法律制度的完善
16.
The package and the label of the imported drugs are inconsistent with those in the documents; Other circumstances not meeting the laws, regulations and rules of the state concerning the control of food and drug.
进口药品包装及标签与单证不符的；其他不符合国家药品监督管理法律、法规和规章规定的。
17.
Analysis of the Laws and Rules of Drug Circulation in China;
我国药品流通领域现行法律法规的剖析
18.
Study on Methods of Adverse Drug Reaction/Event Reporting Assessment
药品不良反应/事件报告评价方法研究