• 家庭预防吸烟法案烟草控制法案赋予美国食品药物管理FDA广泛权力规范烟草产品和营销工作

    The Family Smoking Prevention and Tobacco Control Act gives the Food and Drug Administration (FDA) broad power to regulate tobacco products and marketing efforts.

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  • 美国食品药物管理规范所有婴儿配方奶粉确保它们纯度营养含量达标

    The U.S. Food and Drug Administration regulates all baby formulas to ensure purity and that they meet nutritional requirements.

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  • 一些业务规则需要符合法律规范调整需求比如一些美国通信委员会美国食品及药物管理、联邦航空局1等等制定的规范

    Some business rules are also needed to support legal and regulatory requirements, such as the ones from FCC, FDA, FAA, 1 and so on.

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  • 美国食品药物管理尚未对银杏制剂其它保健品进行规范管理商标不同,药品的效力纯度也不一样。

    Since the Food and Drug Administration do not regulate ginkgo and other supplements, potency and purity vary from brand to brand.

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  • 美国食品和药物管理更多权力规范大型蔬菜农场操作比如科罗拉多农场2011年出售污染哈密瓜

    It gave the FDA more power to regulate operations at large vegetable farms, such as the farm in Colorado that sold contaminated cantaloupes in 2011.

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  • 结论实现抗菌药物使用规范管理提高医疗质量

    CONCLUSIONS the standardized management of antibiotics use is realized and the medical quality is improved.

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  • 药物临床研究必须国家药品监督管理批准实施,必须执行药物临床试验质量管理规范》。

    Clinical study of drugs must be approved by the SDA before it is carried out, and must follow the Criterions for the Quality Control of Clinical Trial of drugs.

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  • 结果促进医护临床药剂师人员之间沟通及药物知识掌握,药品规范管理安全用药

    Results: The communication between nurses and pharmacists improved. They got a lot of knowledge of different medicine, standard medicine management and pathways of safe medication.

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  • 药物安全性评价药物临床安全评价药物非临床研究药物非临床研究质量管理规范即GLP

    The safety evaluation of drugs refers to drugs non-clinical safety evaluation, or drugs non-clinical research, whose quality management practices are called Good Laboratory Practice (GLP).

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  • 第三十二条临床研究药物应当符合《药品生产质量管理规范条件车间制备

    Article 32 Drugs for use in clinical study shall be prepared in workshops meeting the conditions provided for in the Criterions for the Quality Control of Drug Manufacturing.

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  • 结论通过临床药师医院相关部门综合干预,有效促进抗菌药物合理应用规范管理

    Conclusion: Rational use and standard management of antibacterial drugs in hospital can be achieved by participation of clinical pharmacists and other related departments of a hospital.

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  • 新药安全性实验实施质量监督检查药物临床研究质量管理规范(GLP)赋予质量保证部门(QAU)的重要职责

    Study inspection of preclinical safety evaluation of drug is an important responsibility for quality assurance unit (QAU) with good laboratory practice (GLP).

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  • 美国食品药物管理尚未对银杏制剂其它保健品进行规范管理商标不同,药品的效力纯度也不一样。

    Since the Food and Drug Administration do not regulate ginkgo and other supplements, potency and purity vary from brand to brand .

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  • 前言:目的:探讨我国零售药店药物咨询服务规范管理实施对策。

    OBJECTIVE: to seek for the countermeasures to standardize the administration of medical consultation service in the retail pharmacy.

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  • 食品及药物管理宣布了针对人类血液血液组分采集加工存储的药品生产质量管理规范(GMP)。

    The FDA declares Good Manufacturing Practices (GMP) for the collection, processing, and storage of human Blood and Blood components.

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  • 管理患者实施健康宣教自我管理定期随访规范药物治疗等高血压综合管理措施。

    The management group was treated with health education, self management, regular follow-up and standardize the drug treatment.

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  • 结论该院抗菌药物使用尚存在许多问题加强规范化使用管理

    Conclusion Many problems in antimicrobial usage existed, it is important to strengthen standardized administration.

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  • 结论该院抗菌药物使用尚存在许多问题加强规范化使用管理

    Conclusion Many problems in antimicrobial usage existed, it is important to strengthen standardized administration.

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