家庭预防吸烟法案和烟草控制法案赋予美国食品和药物管理局（FDA ）广泛的权力来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.
美国食品与药物管理局规范了所有的婴儿配方奶粉，以确保它们的纯度和营养含量达标。
The U.S. Food and Drug Administration regulates all baby formulas to ensure purity and that they meet nutritional requirements.
一些业务规则还需要符合法律规范和调整的需求，比如一些由美国通信委员会、美国食品及药物管理局、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.
美国食品与药物管理局尚未对银杏制剂和其它保健品进行规范化管理，商标不同，药品的效力和纯度也不一样。
Since the Food and Drug Administration do not regulate ginkgo and other supplements, potency and purity vary from brand to brand.
它给美国食品和药物管理局更多的权力来规范大型蔬菜农场的操作，比如科罗拉多农场在2011年出售污染的哈密瓜。
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.
结论实现抗菌药物使用的规范化管理，提高医疗质量。
CONCLUSIONS the standardized management of antibiotics use is realized and the medical quality is improved.
药物临床研究必须经国家药品监督管理局批准后实施，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.
结果：促进了医护及临床药剂师人员之间的沟通及对药物知识的掌握，药品的规范管理，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.
药物安全性评价是指药物非临床安全评价即药物非临床研究，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).
第三十二条临床研究用药物，应当在符合《药品生产质量管理规范》条件的车间制备。
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.
结论：通过临床药师与医院相关部门的综合干预，可有效促进抗菌药物的合理应用与规范化管理。
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.
对新药安全性实验实施质量监督检查是药物非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).
美国食品与药物管理局尚未对银杏制剂和其它保健品进行规范化管理，商标不同，药品的效力和纯度也不一样。
Since the Food and Drug Administration do not regulate ginkgo and other supplements, potency and purity vary from brand to brand .
前言：目的：探讨我国零售药店药物咨询服务规范化管理的实施对策。
OBJECTIVE: to seek for the countermeasures to standardize the administration of medical consultation service in the retail pharmacy.
食品及药物管理局宣布了针对人类血液和血液组分的采集，加工和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.
对管理组患者实施健康宣教、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.
结论该院抗菌药物使用尚存在许多问题，需加强规范化使用的管理。
Conclusion Many problems in antimicrobial usage existed, it is important to strengthen standardized administration.
结论该院抗菌药物使用尚存在许多问题，需加强规范化使用的管理。
Conclusion Many problems in antimicrobial usage existed, it is important to strengthen standardized administration.
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