药物临床试验,clinical drug trial
1)clinical drug trial药物临床试验
1.The author made a summary about clinical trial management and quality control ofclinical drug trial based on the hospital s practice in recent years.近年来,本院逐步认识到加强药物临床试验的管理,完善质控的重要性。
2.Theclinical drug trial is an important method to assure the effect and security of drug,which means that to confirm or reveal test drugs efficacy and adverse reactions,the researchers conduct a series of clinical trials about new drug effect in human(patients or healthy volunteers).药物临床试验是确定药物疗效和安全性的重要方法。
3.Objective To analyze major factors related to individual expulsion inclinical drug trials and investigate countermeasures to reduce the expulsion rate.目的分析药物临床试验中因受试者个人原因导致不依从的主要因素,探讨降低受试者不依从率的对策。
英文短句/例句
1.The Practices and Opportunities of Hospital Pharmacists in Clinical Trials药师在药物临床试验中的实践与机遇
2.Important role of drug clinical trial institution in quality assurance system药物临床试验机构在药物临床试验质量保证体系中的重要作用
3.Studies on GCP and Supervision for Drug Clinical Trials in China我国GCP与药物临床试验监管研究
4.Brief talk on main points of on-site inspection of drug clinical trial institutions浅谈药物临床试验机构现场检查要点
5.Construction and Management of Drug Clinical Trial Institution in Our Hospital我院药物临床试验机构的建设和管理
6.Opportunities and challenges of scientific monitoring in clinical trials药物临床试验科学监管的机遇与挑战
7.Retrospection and expectation on special column of clinical trials of anti-bacterial drugs《抗菌药物临床试验专栏》的回顾与展望
8.Few Wands of Subjects Protection,Rights and Benefits in Clinical Trials浅析药物临床试验中对受试者的权益保障
9.Application of Xiphophorus Helleri in the Research of Aquatic Pharmaceutical Clinical Experiment;剑尾鱼在水产药物临床试验中应用研究
10.Study on Methodologies for Evaluating Efficacy of Antihypertensive Drug in Clinical Trials;抗高血压药物临床试验疗效评价方法研究
11.Types and main points of site inspections of drug clinical trial institutions in China我国药物临床试验机构现场检查的类型和要点
12.Discussion about standard operating procedures of eye drops clinical trials in ophthalmic clinic眼科门诊药物临床试验标准操作规程探讨
13.Approaches to Improve the Core Competitive Power of Drug Clinical Trial Institutions探索提高药物临床试验机构的核心竞争力
14.Current status and administration for drug clinical trial institutions in Shanghai上海市药物临床试验机构现况及其监管的思考
15.DESIGN AND IMPLEMENTATION OF MANAGEMENT SYSTEM OF DRUG CLINICAL EXAMINATION INFORMATION药物临床试验信息管理系统的设计与实现
16.An Investigation of the Satisfaction of Clinical Research Associate about Drug Clinical Trial Institution Service临床监查员对药物临床试验机构服务的满意度调查
17.International comparison of the monitoring systems of drug safety in clinical trials药物临床试验期间药物安全监控体系的中外比较分析
18.Legal Protection of Subjects Informed Consent in Clinical Drug Trials;浅谈受试者在药物临床试验中知情同意权的法律保护
相关短句/例句
Drug clinical trial药物临床试验
1.Types and main points of site inspections of drug clinical trial institutions in China我国药物临床试验机构现场检查的类型和要点
2.Objective To analyze main causes of drop-out in drug clinical trial and explore the methods of management in reducing its rate.目的分析药物临床试验中影响受试者脱落的主要因素,探讨降低受试者脱落率的管理方法。
3)clinical trial药物临床试验
1.Simulation ofclinical trials: concepts and basic principles;药物临床试验计算机仿真简介
2.The article elucidates the ethical issues inclinical trial, and analyses them with philosophy theory in order to solve the problems in clinical researches.医学伦理学是伴随着科学技术的发展而产生的事物,药物临床试验在促进人类健康事业发展的同时,也涉及到与之相驳的伦理学问题,运用哲学的矛盾原理,浅析药物临床试验与医学伦理之间存在的矛盾及矛盾的两面性,以求解决目前药物临床试验中遇到的困难和问题。
4)good clinical practice药物临床试验管理规范
5)Drug clinical trial institution药物临床试验机构
1.Objective Through the investigation of the satisfaction of Clinical Research Associate(CRA) about drug clinical trial institution service,we explore main influencing factors of the satisfaction.目的:通过对临床监查员关于药物临床试验机构服务满意度的调查,探索影响满意度的主要因素。
6)CTM testing中药临床试验
延伸阅读
临床试验分子式：CAS号：性质：新药的临床试验一般分三期或四期进行。多数国家按四期进行。工期临床试验(phase工Clinical trials)是在人体进行新药试验的起始期。包括药物耐受性(toierance)试验与药代动力学(pharmacokinetics)，生物利用度(bioavailability)研究。Ⅱ期临床试验(phaseⅡ clinicaltrials)要对新药的疗效、适应症、不良反应进行详细考察。通过随机对照临床试验对新药的安全有效性作出确切评价。III期临床试验(phase III clinical trials)为扩大临床试验，目的是在较大范围内对新药的疗效、适应症、不良反应、药物相互作用等进行评价。Ⅳ临床试验(phase IV clinical trials)是在新药投产后进行的，为上市后临床试验或称为上市后药物监察(postmarketing surveillance)。目的是对已在临床广泛应用的新药进行社会性考察，着重于新药的不良反应监察(ad-Verse drug reaction surveillance)。
