FDA consumer consultants are appointed in each field district to maintain communications with consumers and ensure that FDA considers their needs and problems.
在每个辖区任命FDA消费者顾问以保持与消费者的交流，保证FDA能考虑到消费者的需求和问题。
Those will have to be done by FDA employees, an FDA spokesman said today, because the rules for the third-party auditors don't yet exist.
一位食品和药品管理局发言人今日称这些(差事)将由食品和药品管理局的雇员来做，因为针对第三方的条例还未出台。
The FDA goes on to point out that the guidelines from the EPA and the FDA are for drinking water, not for juice.
FDA继续指出，EPA以及FDA公布的标准是相对于饮用水的，而不是对水果汁的。
However, FDA-approval is a long and difficult process, and prior to approval drug manufacturers are prohibited by the FDA from promoting any off-label use of any of their medications to the public.
然而，要得到FDA的批准是一个漫长而艰难的过程，首先是要批准FDA禁止药物制造商促进向公众推荐任何药物治疗的非常规使用这一条款。
This information reflects FDA's current analysis of data available to FDA concerning these products. FDA intends to update this document when additional information or analyses become available.
以上信息反映了FDA对可获得的涉及这些药品的数据的最新分析。一旦有其他信息或分析时，FDA会主动更新该文件。
After Vioxx and other safety controversies, "the American people no longer trust the FDA to protect their health," said Nissen, who has served on FDA advisory panels.
发生了万络和其他安全争议问题之后，“美国民众不在相信FDA能够保护他们的健康，”就职于FDA顾问团的尼森说。
It is essential that companies obtain FDA approval and fully comply with FDA regulations.
因此制药公司必须获得FDA的批准并完全遵从fda的管理。
An FDA plan to revamp the way it inspects imports, called the import Strategic plan, was completed in 2003, but shelved because of budgetary constraints, several former FDA officials said.
几个前FDA官员说，2003年，FDA计划修补进口食品检验方式，被称为“进口战略计划”，但是因为预算局促被搁置。
Methods: Through the analysis and summarization of FDA observation report 483, how to respond to onsite observation from FDA was studied so as to avoid warning letter.
方法通过对FDA现场缺陷报告(483)的分析总结，研究接受FDA现场检查的企业如何合理答复，避免收到FDA警告信。
METHODS Introduce American drug patent system and the method of FDA information retrieval, analyze and ravel out the problems from FDA information retrieval.
方法介绍美国药物专利方面的法规政策及FDA专利情报的检索，并对在FDA及专利数据库检索过程中遇到的问题进行分析。
Chinese citizens are under the impression that the regulation of FDA is very strict, so what approaches does FDA use for regulation of GMO plants and GMO food, and what are the objects of regulation?
的印象是监管很严格，你们对转基因作物、转基因食品采用了什么样的方式监管？ 监管对象都有哪些？
FDA providesinformation to stakeholders on its approval standards and general submissionrecommendations through FDA regulations and guidances [15].
FDA通过FDA法规和指南向关系方提供关于其批准标准和一般申报建议。
"FDA has done considerable work over the past two years to improve our approach to drug safety, and we are committed to taking additional steps," FDA spokeswoman Kristen Neese said.
“过去的两年FDA在提高药物安全方面做了相当多的工作，现在我们正致力于采取更多的步骤，”FDA发言人KristenNeese说。
FDA does not develop or test products; FDA experts review the results of laboratory, animal, and human clinical testing done by manufacturers.
FDA不研发和检测这些制剂，他们的专家只是评价各生厂商在实验室、动物和人临床检验的结果。
FDA spokeswoman Sandy Walsh tells the Health Blog that the materials "were inadvertently posted by the FDA" the first time around.
FDA发言人SandyWalsh告诉健康博客这些材料第一次的时候是“不小心被FDA登载”。
Batavia Solutions, Inc. (Register-FDA department) is specialized in supplying FDA registration, USA FDA agent or any other FDA service for all facility throughout of the world.
FDA部门，致力于为全球范围的出口商提供美国FDA注册、FDA美国代理人或有关FDA事务服务。
In fact, Kessler says television ads never should have been allowed by the FDA in the first place (the FDA legalized drug ads in late 1997, after Kessler left his position there).
Kessler说，实际上药物电视广告从一开始就不应该得到FDA的批准(Kessler离开任职后，FDA在1997年末允许药物广告)。
FDA is considering, but has not reached a final conclusion about, this information. FDA intends to update this sheet when additional information or analyses become available.
FDA考虑到，这不是一个最终的结论，但FDA将在更多资料和有用的分析后更新相关报表。
Facilitate interactions with FDA, including scheduling of FDA inspection.
帮助客户与FDA保持信息互通，包括通知安排验货服务。
Congress authorized FDA to collect an annual establishment registration fee for device establishment registrations submitted to the FDA after September 30th, 2007.
国会授权美国食品和药物管理局收取每年设立登记费为器械设立登记，在2007年9月30日后提交给FDA。
Congress authorized FDA to collect an annual establishment registration fee for device establishment registrations submitted to the FDA after September 30th, 2007.
国会授权美国食品和药物管理局收取每年设立登记费为器械设立登记，在2007年9月30日后提交给FDA。
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