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F.D.A

网络美国食品药物管理局；药品管理局；美国食品医药管理局

F.D.A

网络释义

F.D.A

美国食品药物管理局

美国食品药物管理局（F.D.A）对二氧化钛（光触媒的主要成份）的检测表明它是安全无害的，它不仅可解决室内和车内的污染 …

药品管理局

美国食品与药品管理局（F.D.A）已批准美国出产的可溶性有机活性硒离子可用于口服无毒性无副作用，这种半导体新药可不受 …

美国食品医药管理局

水质电解器也叫固体沉淀促进仪，是经美国食品医药管理局（F.D.A）认定并用来对水质进行基本判定的简易的水质检测方法， …

美国食品药物检验局

‧符合美国食品药物检验局(F.D.A)特等食品级原料精制成。 ‧训练婴儿手脑并用平衡握持。

美国食品暨药物管理局

美国食品暨药物管理局（F.D.A），最近核准必治妥－迈尔斯施贵宝的糖尿病新药glucovance上市，这支药控制血糖效果，可以 …

美国食品药物管理局部

膳食辅助食品。美国食品药物管理局部（F.D.A）通过。

例句：

The F. D. A. does seem to be taking a harder line on new diabetes and heart medicines.

FDA 看起来正在对新的糖尿病药和心脏病药表现出更强硬的态度。

The scandal led Congress to strengthen drug regulations , giving her a role in two of the three seminal events in F. D. A. 's history.

这一丑闻是国会加强了对药品的监管，也是她成为 FDA 历史上三大重要事件中两大事件的亲历者。

The F. D. A. announced in 2007 that it was aware of that problem , but it has taken no action.

食品和药物管理局在 2007年宣布它认识到了那个问题，但它没有采取行动。

Neither of the egg farms had been inspected by the F. D. A. before they were implicated in this outbreak.

而在这次病菌爆发之前也没有一家农场接受过 F.D.A .的检查。

F. D. A. approval of the new drug legitimizes the condition as a problem with a medical solution.

FDA 对这种新药的批准，则给一种医学方法解决健康问题披上了合法外衣。

She and the F. D. A. had a huge role in determining the terms and sequence of what is now modern clinical science.

Kelsey 和 FDA 在确定现代临床规则和条款方面，发挥了重大的作用。

"F. D. A. 's oversight and enforcement efforts have not kept pace with the growing number of food firms, " the report said.

“F.D.A 的疏失及其执行力无法跟上食品公司数量增长的速度，”报告指出。

The F. D. A. gave the advice as it announced a meeting of experts to discuss cold medicines for children.

美国食品与药物管理局是在宣布召开由专家讨论有关儿童感冒药会议时给予的建议。

The F. D. A. generally avoids interfering with the practice of medicine because doctor behavior is governed by state medical boards.

尽量避免干涉医疗行业是因为医生的行为是受联邦医学委员会的管制。

"The F. D. A. set the bar too low on the initial approval , " said Dr. Steven Nissen , chairman of cardiology at the Cleveland Clinic.

“FDA 把初始核准的门槛降得太低了。”StevenNissen 博士说，他是 Cleveland 诊所的心脏病学主席。

Dr. Kelsey might never have reached the F. D. A. in the first place if her first name hadn't sounded like a man's.

若不是她的名字听起来像一个男人的名字，一开始她可能就得不到 FDA 的工作。

Now, sophisticated analyses present the F. D. A. with a complex picture.

现在精密的分析给药品食品局展示出了一幅复杂的图像。

That reputation, in turn, has made the companies that the F. D. A. regulates more willing to respect its authority.

这种尊严反过来也使 FDA 监管的公司更愿意尊重他们的权威。

The F. D. A. plan was also criticized by state officials that regulate the dairy industry.

的这一计划也遭到各州主管奶业官员的批评。

The new labels came after the F. D. A. held two advisory committee meetings to consider the safety of the drugs.

新的标签在 FDA 举行 2 次顾问委员会会议讨论这些药物的安全性之后诞生。

The F. D. A. says most food from cloning is expected to come not from clones themselves , but from their sexually reproduced offspring.

认为大部分克隆食物不是来自克隆本身，而是来自他们的再生同性后代。

The F. D. A. said it would answer the committee 's questions at the hearing.

已经表示他们将在听证会上对能源和商务委员会提出的问题进行回复。

The F. D. A. noted eighteen outbreaks involving fresh or fresh-cut levis (lettuce ) and one involving fresh-cut spinach since 1995.

食品药品管理局注意到自 1995年有十八起大肠杆菌爆发涉及新鲜或现摘的莴苣以及一起现摘菠菜引起的细菌感染。

Only after the F. D. A. inspection did McNeil executives recall millions of bottles of Tylenol, Motrin, Benadryl and other pills.

直到食品药品管理局调查后，麦克尼尔公司才召回了数百万瓶的泰诺、苯那君和其他药品。

Created in 1976 , the F. D. A. 's process for approving devices divides the products into three classes and three levels of scrutiny.

FDA 的医疗设备审核程序创立于 1976年，它把医疗设备划分为三个等级，并且分三级评估。

The F. D. A. must approve an investigatory new drug application before any human testing.

美国食品药品监督管理局一定会在人体试验前批准新药的研究申请。

In the same document , the F. D. A. said it believed that the nation 's milk supply was safe.

同一份文件中，F.D.A 说他们相信国内的牛奶供应是安全的。

For the F. D. A. , the Nissen analysis presented major challenges.

对于药品食品局来说，尼森的分析展现出了较大的挑战。

"As a result , F. D. A. has little assurance that companies comply with food -labeling laws and regulations. "

“因此，F.D.A 无法确保这些公司遵守食品标签法规并服从监管。”

That same year , the F. D. A. finally responded to Dr. Jacobson 's petition.

同一年，食品和药物管理局最终对雅各布森博士的请求作出回应。

It submitted 22 , 000 pages of data to the F. D. A. , perhaps the largest application ever for permission to begin a clinical trial.

该公司向 FDA 提交了一份多大 22,000 页的数据，也许这是允许一项临床试验前提交最多申请的一项试验。

But now , with labs offering more complex tests on a large scale , the F. D. A. is taking a new look at enforcement.

但是现在，这些实验室正在提供更复杂与大规模的试验，使得 FDA 须重新审视规章的执行力度。

It will be given to a F. D. A. staff member annually.

每一年它被将授予给一位食品药品管理局的员工。

But the peer -reviewed clinical trial of 35 patients submitted to the F. D. A. tracked patients for only 90 days.

但是同业临床试验提交美国食品药物管理局的 35 个追踪病例显示维持时间只有 90 天。

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