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1、药物临床试验英文缩写缩略语英文全称中文全称ADEAdverse Drug Event药物不良事件ADRAdverse Drug Reaction药物不良反应AEAdverse Event不良事件AIAssistant Investigator助理研究者BMIBody Mass Index体质指数CICo-investigator合作研究者COICoordinating Investigator协调研究者CRCClinical Research Coordinator临床研究协调者CRFCase Report Form病历报告表CROContract Research Organization合
2、同研究组织CSAClinical Study Application临床研究申请CTAClinical Trial Application临床试验申请CTXClinical Trial Exemption临床试验免责CTPClinical Trial Protocol临床试验方案CTRClinical Trial Report临床试验报告DSMBData Safety and monitoring Board数据安全及监控委员会EDCElectronic Data Capture电子数据米集系统EDPElectronic Data Processing电子数据处理系统FDAFood and D
3、rug Administration美国食品与药品管理局FRFinal Report总结报告GCPGood Clinical Practice药物临床试验质量管理规范GCPGood Laboratory Practice药物非临床试验质量管理规范GMPGood Manufacturing Practice药品生产质量管理规范IBInvestigators Brochure研究者手册ICInformed Consent知情同意ICFInformed Consent Form知情同意书ICHInternational Conference on Harmonization国际协调会议IDMInde
4、pendent Data Monitoring独立数据监察IDMCIndependent Data Monitoring Committee独立数据监察委员会IECIndependent Ethics Committee独立伦理委员会INDInvestigational New Drug新药临床研究IRBInstitutional Review Board机构申查委员会IVDIn Vitro Diagnostic体外诊断IVRSInteractive Voice Response System互动语音应答系统MAMarketing Approval/Authorization上市许可证MCAM
5、edicines Control Agency英国药品监督局MHWMinistry of Health and Welfare日本卫生福利部NDANew Drug Application新药申请NECNew Drug Entity新化学实体NIHNational Institutes of Health国家卫生研究所（美国）缩略语英文全称中文全称PIPrincipal Investigator主要研究者PLProduct License产品许可证PMAPre-market Approval (Application)上市前许可（申请）PSIStatisticians in the Pharma
6、ceutical Industry制药业统计学家协会QAQuality Assurance质量保证QCQuality Control质量控制RARegulatory Authorities监督管理部门SASite Assessment现场评估SAESerious Adverse Event严重不良事件SAPStatistical Analysis Plan统计分析计划SARSerious Adverse Reaction严重不良反应SDSource Data/Document原始数据/文件SDSubject Diary受试者日记SFDAState Food and Drug Administr
7、ation国家食品药品监督管理局SDVSource Data Verification原始数据核准SELSubject Enrollment Log受试者入选表SISub-investigator助理研究者SISponsor-Investigator申办研究者SICSubject Identification Code受试者识别代码SOPStandard Operating Procedure标准操作规程SPLStudy Personnel List研究人员名单SSLSubject Screening Log受试者师选表T&RTest and Reference Product受试和参比试剂U
8、AEUnexpected Adverse Event预料外不良事件WHOWorld Health Organization世界卫生组织WHO-ICDRAWHO International Conference ofDrug Regulatory AuthoritiesWHO国际药品管理当局会议药物临床试验英文缩写英文全称中文全称Accuracy准确度Active control, AC阳性对照活性对照Adverse drug reaction, ADR药物不良反应Adverse event, AE不良事件Adverse medical events不良医学事件Adverse reaction药
9、物不良反应Alb白蛋白ALD (Approximate Lethal Dose)近似致死剂量ALP碱性磷酸酶Alpha spending function消耗函数ALT丙氨酸氨基转换酶Analysis sets统计分析的数据集Approval批准Assistant investigator助理研究者AST天门冬酸氨基转换酶ATR衰减全反射法AUCss稳态血药浓度一时间曲线下面积Audit稽查Audit or inspection稽查/视察Audit report稽查报告Auditor稽查员Bias偏性偏倚Bioequivalence生物等效应Blank control空白对照Blind cod
10、es编制盲底Blind review盲态审核Blind review盲态检杳Blinding method盲法Blinding/masking盲法/设盲Block层Block size每段的长度Carryover effect延滞效应Case history病历Case report form/ case record form CRF病例报告表病例记录表Categorical variable分类变量英文全称中文全称Cav平均浓度CD圆二色谱CL清除率Clinical equivalence临床等效应Clinical study临床研究Clinical study report临床试验的总结
11、报告Clinical trial临床试验Clinical trial application CTA临床试验申请Clinical trial exemption CTX临床试验免责Clinical trial protocol CTP临床试验方案Clinical trial/ study report临床试验报告Cmax峰浓度Co-investigator合作研究者Comparison对照Compliance依从性Composite variable复合变量Computer-assisted trial design CATD计算机辅助试验设计Confidence interval可信区间Co
12、nfidence level置信水平Consistency test一致性检验Contract research organization CRO合同研究组织Contract/ agreement协议/合同Control group对照组Coordinating committee协调委员会Crea肌酐CRF(case report form)病例报告表Crossover design交叉设计Cross-over Study交叉研究Css稳浓度Cure痊愈Data management数据管理Database建立数据库Descriptive statistical analysis描述性统计分
13、析DF波动系统Dichotomies二分类Diviation偏差Documentation记录/文件英文全称中文全称Dose-reaction relation剂量一反应关系Double dummy双模拟Double dummy technique双盲双模拟技术Drop out脱落DSC差示扫描热量计Effectiveness疗效Electronic data capture EDC电子数据米集系统Electronic data processing EDP电子数据处理系统Emergency envelope应急信件End point终占k、八、Endpoint Criteria终点指标Endpoint criteria/ measurement终点指标Equivalence等效性Essential Documentation必需文件Ethics committee伦理委员会Excellent显效Exclusion criteria排除标准Factorial design析因设计Failure无效失败Final point终占k、八、Fixed-dose procedure固定剂量法Forced titration强制滴定Full analysis set全分析集GC-FTIR气相色谱一傅利叶红外联用GC-MS气相色谱质谱联用
