有四种药物注册用于治疗昏睡病并免费向疾病流行国家提供。
Four drugs are registered for the treatment of sleeping sickness and provided free of charge to endemic countries.
新药物在临床试验期间接受有限的安全性评估后，即正式注册并投放市场；在大规模普遍使用过程中，只能出现极为罕见的意外的副作用个案。
New medicines are registered and enter the market with limited safety evaluation during clinical trials; rare unexpected side effects can only be detected during large-scale use.
然而即使没有这个专门分类，批准该类知识产权的可能已经引发是否应允许长期使用的药物名称注册商标的激烈争议。
But even in the absence of a dedicated grouping, the prospect of intellectual property approval has sparked a vigorous debate over whether long-used names for the drug can be trademarked.
许多丙肝病毒专用口服药物也处于开发后期，有一些药物最近已获得注册。
A great number of HCV specific oral drugs are in the late stage of development; some have been recently registered.
在公司实体购买药物之前，你应该确定药物调制的特定场所是有满意检查结果的已注册的外包场所。
Before purchasing drugs from a corporate entity, you should determine that the specific facility in which the drugs are compounded is a registered outsourcing facility with a satisfactory inspection.
工业药剂师从事药物和相关供应品开发、生产、储存、质量控制和分配方面的研究、测试和分析。需要注册或许可。
Undertakes research, testing and analysis related to the development, production, storage, quality control and distribution of drugs and related supplies. Registration or licensing is required.
在临床试验注册网站查询未公布的试验数据，对上交到美国食品与药物管理局的与福莫特罗有关的资料也进行查证。
Web sites of clinical trial registers were checked for unpublished trial data and Food and Drug Administration submissions in relation to formoterol were also checked.
酰胺是非注册药物退热净的专卖形式。
Acetaminophen 'is the generic form of the proprietary drug' Tylenol '.
本周，保守党将保证，抗癌药物一经注册，将向所有患者提供。
This week the Conservatives will issue a pledge to make cancer drugs available to all as soon as they are licensed.
文中结合化学药物制剂处方工艺的研究及其注册申报中一些有代表性的问题，尝试对《化学药物制剂研究基本技术指导原则》相关内容进行解读。
"Guidance for Pharmaceutical Development of Chemical Drug Products" was interpreted herein based on analysis of the typical problems occurred in registration of chemical drug products.
食品与药品管理局已经接受该公司的新药申请并将文件归档，而且还组织了处方药物使用权行动，活动目标是将公司新药注册日期定在2008年一月二十三日。
The FDA has accepted the Company's NDA for filing and has set a Prescription Drug User Fee act (PDUFA) target action date for the Company's NDA of January 23, 2008.
食品与药品管理局已经接受该公司的新药申请并将文件归档，而且还组织了处方药物使用权行动，活动目标是将公司新药注册日期定在2008年一月二十三日。
The FDA has accepted the Company's NDA for filing and has set a Prescription Drug User Fee act (PDUFA) target action date for the Company's NDA of January 23, 2008.
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