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- Preventive drug application 预防用药
- Investigational New Drug Application (IND) for the compound. 为化合物的研究中的新药物申请 (IND)。
- FDA said, companies that intend to market nicotine water should submit a new drug application to the agency for review. 食品暨药物管理局说,想要在市场上贩卖菸草水的公司,应向该局提出新的药品上市申请书,以便审核。
- But the preventive drugs have a risk of sidy factsside effects. 但是预防的药品由副作用的危险。
- AIM:To study the effects of the extract of Equisetum Hiemale on platelet aggregation and thrombosis so as to provide experimental basis for preventive drug intervention of stroke. 目的:研究木贼提取物对血小板聚集和血栓形成的影响,以期为脑卒中预防ntg药物干预提供实验基础。
- CONCLUSION:Ratio ordering method deserves to be generalization and application in drug application&taking by compute... 结论比值排序法是一种值得推广应用的药房药品计算机申领方法。
- Methods nature fade were divided into 7 groups.Sodium nitrite and dexamethasone were injection via abdominal,preventive drug was used in other normal control group. 方法将小鼠随机分为7组,除正常对照组外,给予自然衰老及腹腔注射亚硝酸钠和地塞米松处置,给药组预防性给药。
- Objective: To study the macrolide antibiotic adverse reaction and safety of drug application. 目的:探讨大环内酯类抗生素的不良反应及用药安全性。
- Another concept is to prevent drug resistance and optimal management of strategy was nucleoside resistance mutation. 而另一种观念是阻止耐药的发生。
- Regulatory Submissions in Electronic Format; New Drug Applications. 以电子格式递交申请:新药申请。
- Clinical trials conducted between regulatory submission of an NDA (New Drug Application) and approval of a regulatory dossier for marketing authorization. 旨在向药审机构递交了新药注册申请之后到申请药物被批准上市之前的一段时间内进行的相关药物临床试验.
- Formulation Researcher:1.Ph D. or master in formulation;2.Fluent in preformulation study;3.Persons of drug application e...... ... 公司名称:永信药品工业(昆山)有限公司工作地点:江苏省苏州市昆山市发布时间:2009-7-25
- Objective: To know about the matter on the anaphylactic shock caused by quinolone series, so as to provide references for drug application clinically. 目的:了解喹诺酮类药物致过敏性休克的情况,为临床用药的安全性提供参考。
- It applies to the life of a drug from Investigational New Drug (IND), New Drug Application (NDA), post-marketing, and even removal from markedng. 方法利用文献资料采取综述的方法,介绍药品风险管理概念在美国、欧盟的发展和药品风险管理的内容。
- Clinical trials conducted between regulatory submission of an NDA( New Drug Application) and approval of a regulatory dossier for marketing authorization. 旨在向药审机构递交了新药注册申请之后到申请药物被批准上市之前的一段时间内进行的相关药物临床试验.
- Generic drug application reviewers focus on bioequivalence data, chemistry and microbiology data, requests for plant inspection, and drug labeling information. 仿制药申请的的评审官着重于生物等效性资料,化学和生物资料,工厂检查的要求和药品标签信息等。
- Dronedarone is manufactured by Sanofi-Aventis.A new drug application was filed in June 2005 and is currently under review by the US Food and Drug Administration. 他附带表示,未来需要这2个药物互相比较的临床试验,但是这将需要非常大的试验样本。
- After reiewing the issues raised in the petition, FDA determined that its standards for approal of the generic drug application for bupropion are appropriate. FDA审查请愿书中的问题后确认,其批准盐酸安非他酮仿制药申请的标准是恰当的。
- This process allows a company to file the sections of the New Drug Application (NDA) as they become available instead of filing all the sections at once. 这个过程允许公司提交的新药申请(NDA),因为它们变得可用,而不是提出在一旦所有的部分章节。
- Statins plays a role in reducing blood LDL cholesterol,acting as a second-level prevention drug for coronary artery disease. 目的他汀类药物具有肯定的降脂作用,已作为冠状动脉粥样硬化性心脏病的二级预防用药。