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Drug Administration Law

  • 《药品管理法》

网络释义专业释义

  药品管理法

... 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 ...

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短语

newly revised drug administration law 新修订

law of drug administration 药品管理法

law drug administration 药品管理法

drug medical devices administration law 药品监督执法

 更多收起网络短语
  • 药品管理法

·2,447,543篇论文数据,部分数据来源于NoteExpress

双语例句权威例句

  • 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

    youdao

  • 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.

    结果结论现行《药品管理法中的假药定义不能有效地适用各种类型药品假药判定,需要进行改进。

    youdao

  • The new law gives the US Food and Drug Administration the power to strictly limit the manufacturing and marketing of tobacco products.

    新的法律美国食品药品生产烟草的生产市场带来很大的限制

    youdao

更多双语例句
  • Repeal the DSHEA law and give the Food and Drug Administration full authority over every manufactured substance that purports to promote health or relieve illness.

    CNN: Herbal remedies need real scrutiny

  • But the Food and Drug Administration does not prospectively review food claims because American law says that foods are allowed to affect the "structure and function" of the body, so long as they do not actually claim to treat disease.

    FORBES: Magazine Article

  • Investigators for the state's DPH, working with their counterparts at the U.S. Food and Drug Administration, "identified serious deficiencies and significant violations of pharmacy law and regulations that clearly placed the public's health at risk, " it said.

    CNN: STORY HIGHLIGHTS

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