药物临床试验英文缩写

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 React ion药物不良反应AEAdverse Event不良事件AIAssista nt In vestigator助理研究者BMIBody Mass In dex体质指数CICo-i nvestigator合作研究者COICoordin at ing In vestigator协调研究者CRCCli ni cal Research Coordin ator临床研究协调者CRFCase Report Form病历报告表CROCon tract Research O

2、rga ni zatio n合同研究组织CSACli ni cal Study Applicati on临床研究申请CTAClinical Trial Application临床试验申请CTXCli nical Trial Exempti on临床试验免责CTPCli nical Trial Protocol临床试验方案CTRCli nical Trial Report临床试验报告DSMBData Safety and mon itori ng Board数据安全及监控委员会EDCElectronic Data Capture电子数据采集系统EDPElectr onic Data Proces

3、s ing电子数据处理系统FDAFood and Drug Adm ini strati on美国食品与药品管理局FRFinal Report总结报告GCPGood Cli nical Practice药物临床试验质量管理规GCPGood Laboratory Practice药物非临床试验质量管理规GMPGood Manu facturi ng Practice药品生产质量官理规IBInvestigator s Brochure研究者手册ICIn formed Consent知情同意ICFIn formed Consent Form知情冋意书ICHIntern ati onalConfere

4、nceonHarmoni zati on国际协调会议IDMIn depe ndent Data Mon itori ng独立数据监察IDMCIn depe ndent Data Mon itori ng Committee独立数据监察委员会IECIn depe ndent Ethics Committee独立伦理委员会INDIn vestigati onal New Drug新药临床研究IRBInstitutional Review Board机构审查委员会IVDIn Vitro Diag no stic体外诊断IVRSIn teractive Voice Resp onse System互动

5、语音应答系统MAMarketing Approval/Authorization上市许可证MCAMedici nes Con trol Age ncy英国药品监督局MHWMin istry of Health and Welfare日本卫生福利部NDANew Drug Applicati on新药申请NECNew Drug En tity新化学实体缩略语英文全称中文全称NIHNational Institutes of Health国家卫生研究所（美国）PIPrin cipal In vestigator主要研究者PLProduct Lice nse产品许可证PMAPre-market App

6、roval (Applicati on)上市前许可（申请）PSIStatisticia ns inthe PharmaceuticalIn dustry制药业统计学家协会QAQuality Assura nee质量保证QCQuality Con trol质里控制RARegulatory Authorities监督管理部门SASite Assessme nt现场评估SAESerious Adverse Event严重不良事件SAPStatistical An alysis Pla n统计分析计划SARSerious Adverse React ion严重不良反应SDSource Data/Doc

7、ume nt原始数据/文件SDSubject Diary受试者日记SFDAState Food and Drug Admi nistrati on国家食品药品监督管理局SDVSource Data Verificati on原始数据核准SELSubject En rollme nt Log受试者入选表SISub-i nvestigator助理研究者SISponsor-In vestigator申办研究者SICSubject Identification Code受试者识别代码SOPStan dard Operati ng Procedure标准操作规程SPLStudy Personnel Li

8、st研究人员SSLSubject Scree ning Log受试者帅选表T&RTest and Refere nee Product受试和参比试剂UAEUn expected Adverse Event预料外不良事件WHOWorld Health Orga ni zati on世界卫生组织WHO-ICDRAWHO Intern ati onal Conference ofDrug Regulatory AuthoritiesWHO!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 con trol, AC阳性对照活性对照Adverse drug rea

9、ctio n, ADR药物不良反应Adverse eve nt, AE不良事件Adverse medical events不良医学事件Adverse react ion药物不良反应Alb白蛋白ALD (Approximate Lethal Dose )近似致死剂量ALP碱性磷酸酶Alpha spe nding function消耗函数ALT丙氨酸氨基转换酶An alysis sets统计分析的数据集Approval批准Assista nt in vestigator助理研究者AST天门冬酸氨基转换酶ATR衰减全反射法AUCss稳态血药浓度时间曲线下面积Audit稽查Audit or in sp

10、ect ion稽查/视察Audit report稽查报告Auditor稽查员Bias偏性偏倚Bioequivale nee生物等效应Blank con trol空白对照Bli nd codes编制盲底Bli nd review盲态审核Bli nd review盲态检杳Bli nding method盲法Bli ndin g/mask ing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英文全称中文全称Categorical v

11、ariable分类变量Cav平均浓度CD圆二色谱CL清除率Cli ni cal equivale nee临床等效应Cli ni eal study临床研究Cli ni eal study report临床试验的总结报告Clinical trial临床试验Clinical trial application CTA临床试验申请Cli nical trial exemption CTX临床试验免责Clinical trial protocol CTP临床试验方案Cli ni cal trial/ study report临床试验报告Cmax峰浓度Co-i nvestigator合作研究者Compa

12、ris on对照Complia nee依从性Composite variable复合变量Computer-assisted trial desig n CATD计算机辅助试验设计Con fide nee in terval可信区间Con fide nee level置信水平Con siste ncy test一致性检验Con tract research orga ni zati on CRO合同研究组织Con tract/ agreeme nt协议/合同Con trol group对照组Coordin at ing committee协调委员会Crea肌酐CRF(case report fo

13、rm)病例报告表Crossover desig n交叉设计Cross-over Study交叉研究Css稳浓度Cure痊愈Data man ageme nt数据管理Database建立数据库Descriptive statistical an alysis描述性统计分析DF波动系统Dichotomies二分类Diviatio n偏差英文全称中文全称Docume ntati on记录/文件Dose-react ion relati on剂量-反应关系Double dummy双模拟Double dummy tech nique双盲双模拟技术Drop out脱落DSC差示扫描热量计Effective

14、 ness疗效Electro nic data capture EDC电子数据采集系统Electr onic data process ing EDP电子数据处理系统Emerge ncy en velope应急信件End point终占八、En dpo int Criteria终点指标Endpoint criteria/ measurement终点指标Equivale nee等效性Esse ntial Docume ntatio n必需文件Ethics committee伦理委员会Excelle nt显效Exclusion criteria排除标准Factorial desig n析因设计Fa

15、ilure无效失败Final point终占八、Fixed-dose procedure固定剂量法Forced titrati on强制滴定Full an alysis set全分析集GC- FTIR气相色谱-傅利叶红外联用GC- MS气相色谱-质谱联用Gen eric drug通用名药Global assessme nt variable全局评价变量GLU血糖Good cli ni cal practice, GCP药物临床试验质量管理规Good manufacture practice, GMP药品生产质量官理规Good non-cli ni cal laboratory practice

16、, GLP药物非临床研究质量官理规Group seque ntial desig n成组序贯设计Health econo mic evaluati on, HEV健康经济学评价Hypothesis test假设检验Hypothesis test ing假设检验英文全称中文全称Improveme nt好转In clusi on Criteria入选表准Inclusion criteria入选标准In depe ndent ethics committee IEC独立伦理委员会Information consent form ICF知情冋意书Information Gathering信息收集In

17、formed consent IC知情同意In itial meet ing启动会议In spect ion检察/视察In stituti on in specti on机构检查In stituti on review board, IBR机构审查委员会Inten tio n-to treat ITT意向性分析（统计学）In teractive voice resp onse system IVRS互动式语音应答系统In terim an alysis期中分析Intern ati onalConferenceofHarmoni zati on ICH人用药品注册技术要求国际技术协调会国际协调会

18、议In vestigati onal Product试验药物In vestigator研究者Investigator s brochure, IB研究者手册Last observati on carry forward, LOCF最接近一次观祭的结转LC MS液相色谱-质谱联用LD50板数致死剂量LOCF, Last observati on carry forward最近一次观祭的结转Logic check逻辑检杳LOQ (Limit of Qua ntizati on)定量限Lost of follow up失访Marketing approval/ authorization上市许可证M

19、atched pair匹配配对Miss ing value缺失值Mixed effect model混合效应模式Mo nitor监察员Mon itori ng监杳Monitoring Plan监察计划Monitoring Report监察报告MRT平均滞留时间MS质谱MS- MS质谱-质谱联用英文全称中文全称MTD( Maximum Tolerated Dose )最大耐受剂量Multi-ce nter Trial多中心试验New chemical en tity NCE新化学实体New drug application NDA新药申请NMR核磁共振谱Non-clinical Study非临床

20、研究Non-i nferiority非劣效性Non-parametric statistics非参数统计方法Obedie nee依从性ODR旋光光谱Open-label非盲Optio nal titratio n随意滴定Origi nal medical record原始医疗记录Outcome结果Outcome Assessme nt结果评价Outcome assessme nt结果指标评价Outcome measureme nt结果指标Outlier离群值Parallel group desig n平行组设计Parameter estimati on参数估计Parametric statis

21、tics参数统计方法Patient file病人档案Patie nt history病历Per protocol PP符合方案集Placebo安慰剂Placebo con trol安慰剂对照Polytomies多分类Power检验效能Precisi on精密度Precli nical study临床前研究Primary en dpo int主要终点Primary variable主要变量Prin ciple in vestigator PI主要研究者Product lice nse PL产品许可证Protocol试验方案Protocol Ame ndme nts修正案Quality assur

22、a nee QA质量保证英文全称中文全称Quality assura nee un it QAU质量保证部门Quality control QC质量控制Query list query form应用疑问表Ran domizati on随机Range check围检查Rati ng scale量表Refere nee Product参比制剂Regulatory authorities RA监督管理部门Replicati on可重复RSD日和日间相对标准差Run in准备期Safety evaluati on安全性评价Safety set安全性评价的数据集Sample size样本量样本大小Sca

23、le of ordered categorical rat ings有序分类指标Secon dary variable次要变量Sequenee试验次序Serious adverse event SAE严重不良事件Serious adverse reacti on SAR严重不良反应Serious ness严重性Severity严重程度Severity严重程度Signi fica nt level检验水准Simple Ran domizatio n简单随机Si ngle bli nding单盲Site audit试验机构稽查SOP试验室的标准操作规程Source data SD原始数据Sourc

24、e data verificatio n SDV原始数据核准Source docume nt SD原始文件Specificity特异性Sponsor申办者Sponsor-in vestigator申办研究者Stan dard curve标准曲线Stan dard operati ng procedure SOP标准操作规程Statistic统计量Statistical an alysis pla n统计分析计划英文全称中文全称Statistical model统计模型Statistical tables统计分析表Stratified分层Study Audit研究稽查Study audit研究稽

25、查Study Site研究中心Subgroup亚组Sub-i nvestigator助理研究者Subject受试者Subject受试者Subject diary受试者日记Subject En rollme nt受试者入选Subject en rollme nt log受试者入选表Subject ide ntificati on code SIC受试者识别代码Subject Ide ntificati on Code List受试者识别代码表Subject Recruitme nt受试者招募Subject scree ning log受试者师选表Superiority检验Survival an

26、alysis生存分析SXRD单晶X-射线衍射System audit系统稽查System Audit系统稽查T1/2消除半衰期Target variable目标变量T- BIL总胆红素T- CHO总胆固醇Test Product受试制剂TG热重分析TLC HPLC制备色谱Tmax峰时间TP总蛋白Tran sformatio n变量变换Treatme nt group试验组Trial error试验误差Trial In itial Meet ing试验启动会议Trial Master File试验总档案Trial objective试验目的英文全称中文全称Trial site试验场所Triple

27、 bli nding二盲Two on e-side test双单侧检验Un-bli nding揭盲Un expected adverse eve nt UAE预料外不良事件UV VIS紫外-可见吸收光谱Variability变异Variable变量Visual an alogy scale直观类比打分法Visual check人工检查Vuln erable subject弱势受试者Wash-out洗脱Washout period洗脱期实验室检查英文缩写英文全称中文全称血常规WBC white blood cell cou nt白细胞计数GR% granu locyte中性粒细胞百分比LY% l

28、ymphocyte淋巴细胞百分比MID%中值细胞百分比EOS% eosimophil嗜酸性粒细胞百分比AL% allergy lymphocyte变异淋巴细胞百分比ST%中性杆状粒细胞百分比RBC red blood cell红细胞计数HGB hemoglobi n血红蛋白HCT hematocrit 红细胞比积红细胞比积MCV mean corpusular volume平均红细胞体积MCH mea n corpusular hemoglob in平均红细胞血红蛋白含量MCHC mea ncorpusularhemoglob inconcern trati on平均红细胞血红蛋白浓度RDW

29、red blood cell volume distributi on width红细胞分布宽度变异PLT/BPC plateletcount/blood plateletcou nt血小板计数MPV mea n platelet volume平均血小板体积PCT plateletocrit血小板比积PDW platelet distribution width血小板分布宽度尿便常规PH acidity酸碱度NIT nitrite亚硝酸盐GLU glucose尿糖SG specific gravity比重PRO protein尿蛋白BLD blood隐血BIL bilirubi n尿胆红素UR

30、O urobil inogen尿胆原WBC white blood cell白细胞addish 计数 addish count艾迪氏计数/HP high power objective每高倍视野/LP low power objective每低倍视野英文全称中文全称OB occult blood test大便隐血试验体液常规CSF cerebrosp inal脑积夜Pandy pandy庞氏试验生化检验TB total bilirubin总胆红素DB direct bilirub in直接胆红素TP total protein总蛋白ALB albumin白蛋白GLOB globulin球蛋白U

31、REA urea尿素CREA creati nine肌肝UA uric acid尿酸GLU glucose血糖ALT ala nine amiotra nsferase丙氨酸氨基转移酶AST aspartate aminotran sferase门冬氨酸氨基转移酶GGT Y -glutamyl transpeptadase谷氨酰转肽酶CK creat ine kin ase肌酸肌酶CK-MB creati ne kin ase-MB肌酸肌酶同工酶LDH lactate dehydroge nase乳酸脱氢酶a -HBD a -hydroxybutyric dehydrogenasea 羟丁酸脱氢酶AMY serum amylase血淀粉酶TG triglyceride肝油三脂CHOL cholesterol胆固醇HDL-chigh-de nsitylipoproteincholesterol高密度脂蛋白LDL-clow-de nsitylipoproteincholester