]> 2026-08-03T16:46:44+00:00 Clinical research 14 en 2007-09-12T07:36:15Z 2454355.8168403 Clinical research Food and Drug Administration 0 en Food and Drug Administration Caco-2 0 en Caco-2 Excipient 0 en Excipient Covered clinical study 0 en Covered clinical study Drug design 0 en Drug design Clinical site 0 en Clinical site Regulatory requirement 0 en Regulatory requirement Investigational product 0 en Investigational product Nonclinical studies 0 en Nonclinical studies Source document 0 en Source document Quality management system 0 en Quality management system New drug application 0 en New drug application Crossover study 0 en Crossover study Clinical trial 0 en Clinical trial Clinical investigator 0 en Clinical investigator Institutional Review Board 0 en Institutional Review Board Pharmaceuticals in India 0 en Pharmaceuticals in India Randomized controlled trial 0 en Randomized controlled trial Placebo 0 en Placebo Contract research organization 0 en Contract research organization Blind experiment 0 en Blind experiment Drug discovery 0 en Drug discovery Institute for OneWorld Health 0 en Institute for OneWorld Health Effect size 0 en Effect size Inclusion criteria 0 en Inclusion criteria Exclusion criteria 0 en Exclusion criteria Clinical monitoring 0 en Clinical monitoring Multicenter trial 0 en Multicenter trial Standard treatment 0 en Standard treatment Assay sensitivity 0 en Assay sensitivity Clinical baseline 0 en Clinical baseline Safety monitoring 0 en Safety monitoring Serious adverse event 0 en Serious adverse event Investigational Device Exemption 0 en Investigational Device Exemption InSilico modeling 0 en InSilico modeling Therapeutics Goods Administration 0 en Therapeutics Goods Administration South African Health Ministry 0 en South African Health Ministry Adverse event 0 en Adverse event Validation (drug manufacture) 0 en Validation (drug manufacture) European Forum for Good Clinical Practice 0 en European Forum for Good Clinical Practice Remote Data Entry 0 en Remote Data Entry Norwegian Medicines Agency 0 en Norwegian Medicines Agency European Medicines Agency 0 en European Medicines Agency State Food and Drug Administration 0 en State Food and Drug Administration Approved drug 0 en Approved drug Standing operating procedure 0 en Standing operating procedure Good clinical practice 0 en Good clinical practice Clinical trial management 0 en Clinical trial management First-in-man study 0 en First-in-man study Medical Products Agency 0 en Medical Products Agency Council for International Organizations of Medical Sciences 0 en Council for International Organizations of Medical Sciences CIOMS Guidelines 0 en CIOMS Guidelines Indian health ministry 0 en Indian health ministry World Medical Association 0 en World Medical Association EudraVigilance 0 en EudraVigilance Drug Efficacy Study Implementation 0 en Drug Efficacy Study Implementation Kefauver Harris Amendment 0 en Kefauver Harris Amendment Directive 65/65/EEC1 0 en Directive 65/65/EEC1 EudraLex 0 en EudraLex Qualified Person 0 en Qualified Person Directive 93/41/EEC 0 en Directive 93/41/EEC Directive 2001/83/EC 0 en Directive 2001/83/EC Directive 2001/20/EC 0 en Directive 2001/20/EC Directive 2005/28/EC 0 en Directive 2005/28/EC EUDRANET 0 en EUDRANET EudraGMP 0 en EudraGMP EudraPharm 0 en EudraPharm Ministry of Health, Labour and Welfare (Japan) 0 en Ministry of Health, Labour and Welfare (Japan) Therapeutic Products Directorate 0 en Therapeutic Products Directorate International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use 0 en International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Bioequivalence 0 en Bioequivalence Unified Parkinson's Disease Rating Scale 0 en Unified Parkinson's Disease Rating Scale Boston Collaborative Drug Surveillance Program 0 en Boston Collaborative Drug Surveillance Program Academic clinical trials 0 en Academic clinical trials Clinical trials publication 0 en Clinical trials publication Harmonization in clinical trials 0 en Harmonization in clinical trials Run-in period 0 en Run-in period European and Developing Countries Clinical Trials Partnership 0 en European and Developing Countries Clinical Trials Partnership National Guideline Clearinghouse 0 en National Guideline Clearinghouse Post-randomized consent 0 en Post-randomized consent Resentful demoralization 0 en Resentful demoralization Post-hoc analysis 0 en Post-hoc analysis Data Monitoring Committees 0 en Data Monitoring Committees Operation Whitecoat 0 en Operation Whitecoat Clinical trial protocol 0 en Clinical trial protocol Clinical Data Interchange Standards Consortium 0 en Clinical Data Interchange Standards Consortium Case Report Form 0 en Case Report Form Patient-reported outcome 0 en Patient-reported outcome Data clarification form 0 en Data clarification form Investigator's Brochure 0 en Investigator's Brochure Belmont Report 0 en Belmont Report Common Technical Document 0 en Common Technical Document Clinical data management system 0 en Clinical data management system EudraCT 0 en EudraCT Patient Diary 0 en Patient Diary Clinical Trial Management System 0 en Clinical Trial Management System Electronic Common Technical Document 0 en Electronic Common Technical Document De Novo Software 0 en De Novo Software Clinical research associate 0 en Clinical research associate Project 112/shad 0 en Project 112/shad Institute of Food and Agricultural Sciences 0 en Institute of Food and Agricultural Sciences Trier Social Stress Test 0 en Trier Social Stress Test Informed consent 0 en Informed consent Minimisation 0 en Minimisation Crtn 0 en Crtn Electronic data capture 0 en Electronic data capture Whole systems research 0 en Whole systems research Clinical research organization 0 en Clinical research organization Postmarketing surveillance 0 en Postmarketing surveillance Study of Tamoxifen and Raloxifene 0 en Study of Tamoxifen and Raloxifene Ethics Committee (European Union) 0 en Ethics Committee (European Union) National Commission for the Protection of Human Subjects of Biomedical and Behavioral Research 0 en National Commission for the Protection of Human Subjects of Biomedical and Behavioral Research Good Clinical Data Management Practice 0 en Good Clinical Data Management Practice ACUITY 0 en ACUITY GUSTO 0 en GUSTO CURE 0 en CURE HORIZONS 0 en HORIZONS STEEPLE 0 en STEEPLE PLATO 0 en PLATO GRACE 0 en GRACE Placebo-controlled studies 0 en Placebo-controlled studies Provocation study 0 en Provocation study Carvedilol Post Infarct Survival Control in Left Ventricular Dysfunction Study 0 en Carvedilol Post Infarct Survival Control in Left Ventricular Dysfunction Study GUSTO-I 0 en GUSTO-I Institutional review board 0 en Institutional review board Clinomics 0 en Clinomics Pharmacology 14 en Pharmacology Medical research 14 en Medical research Food and Drug Administration 14 en Food and Drug Administration Experimental medical treatments 14 en Experimental medical treatments Clinical trials 14 en Clinical trials Biotechnology 14 en Biotechnology Drug discovery 14 en Drug discovery Clinical Data Management 14 en Clinical Data Management Contract research organizations 14 en Contract research organizations ACUITY 0 en ACUITY Academic clinical trials 0 en Academic clinical trials Adverse event 0 en Adverse event Approved drug 0 en Approved drug Assay sensitivity 0 en Assay sensitivity Belmont Report 0 en Belmont Report Bioequivalence 0 en Bioequivalence Blind experiment 0 en Blind experiment Boston Collaborative Drug Surveillance Program 0 en Boston Collaborative Drug Surveillance Program CIOMS Guidelines 0 en CIOMS Guidelines CURE 0 en CURE Caco-2 0 en Caco-2 Carvedilol Post Infarct Survival Control in Left Ventricular Dysfunction Study 0 en Carvedilol Post Infarct Survival Control in Left Ventricular Dysfunction Study Case Report Form 0 en Case Report Form Clinical Data Interchange Standards Consortium 0 en Clinical Data Interchange Standards Consortium Clinical Trial Management System 0 en Clinical Trial Management System Clinical baseline 0 en Clinical baseline Clinical data management system 0 en Clinical data management system Clinical investigator 0 en Clinical investigator Clinical monitoring 0 en Clinical monitoring Clinical research associate 0 en Clinical research associate Clinical research organization 0 en Clinical research organization Clinical site 0 en Clinical site Clinical trial 0 en Clinical trial Clinical trial management 0 en Clinical trial management Clinical trial protocol 0 en Clinical trial protocol Clinical trials publication 0 en Clinical trials publication Clinomics 0 en Clinomics Common Technical Document 0 en Common Technical Document Contract research organization 0 en Contract research organization Council for International Organizations of Medical Sciences 0 en Council for International Organizations of Medical Sciences Covered clinical study 0 en Covered clinical study Crossover study 0 en Crossover study Crtn 0 en Crtn Data Monitoring Committees 0 en Data Monitoring Committees Data clarification form 0 en Data clarification form De Novo Software 0 en De Novo Software Directive 2001/20/EC 0 en Directive 2001/20/EC Directive 2001/83/EC 0 en Directive 2001/83/EC Directive 2005/28/EC 0 en Directive 2005/28/EC Directive 65/65/EEC1 0 en Directive 65/65/EEC1 Directive 93/41/EEC 0 en Directive 93/41/EEC Drug Efficacy Study Implementation 0 en Drug Efficacy Study Implementation Drug design 0 en Drug design Drug discovery 0 en Drug discovery EUDRANET 0 en EUDRANET Effect size 0 en Effect size Electronic Common Technical Document 0 en Electronic Common Technical Document Electronic data capture 0 en Electronic data capture Ethics Committee (European Union) 0 en Ethics Committee (European Union) EudraCT 0 en EudraCT EudraGMP 0 en EudraGMP EudraLex 0 en EudraLex EudraPharm 0 en EudraPharm EudraVigilance 0 en EudraVigilance European Forum for Good Clinical Practice 0 en European Forum for Good Clinical Practice European Medicines Agency 0 en European Medicines Agency European and Developing Countries Clinical Trials Partnership 0 en European and Developing Countries Clinical Trials Partnership Excipient 0 en Excipient Exclusion criteria 0 en Exclusion criteria First-in-man study 0 en First-in-man study Food and Drug Administration 0 en Food and Drug Administration GRACE 0 en GRACE GUSTO 0 en GUSTO GUSTO-I 0 en GUSTO-I Good Clinical Data Management Practice 0 en Good Clinical Data Management Practice Good clinical practice 0 en Good clinical practice HORIZONS 0 en HORIZONS Harmonization in clinical trials 0 en Harmonization in clinical trials InSilico modeling 0 en InSilico modeling Inclusion criteria 0 en Inclusion criteria Indian health ministry 0 en Indian health ministry Informed consent 0 en Informed consent Institute for OneWorld Health 0 en Institute for OneWorld Health Institute of Food and Agricultural Sciences 0 en Institute of Food and Agricultural Sciences Institutional Review Board 0 en Institutional Review Board Institutional review board 0 en Institutional review board International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use 0 en International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Investigational Device Exemption 0 en Investigational Device Exemption Investigational product 0 en Investigational product Investigator's Brochure 0 en Investigator's Brochure Kefauver Harris Amendment 0 en Kefauver Harris Amendment Medical Products Agency 0 en Medical Products Agency Minimisation 0 en Minimisation Ministry of Health, Labour and Welfare (Japan) 0 en Ministry of Health, Labour and Welfare (Japan) Multicenter trial 0 en Multicenter trial National Commission for the Protection of Human Subjects of Biomedical and Behavioral Research 0 en National Commission for the Protection of Human Subjects of Biomedical and Behavioral Research National Guideline Clearinghouse 0 en National Guideline Clearinghouse New drug application 0 en New drug application Nonclinical studies 0 en Nonclinical studies Norwegian Medicines Agency 0 en Norwegian Medicines Agency Operation Whitecoat 0 en Operation Whitecoat PLATO 0 en PLATO Patient Diary 0 en Patient Diary Patient-reported outcome 0 en Patient-reported outcome Pharmaceuticals in India 0 en Pharmaceuticals in India Placebo 0 en Placebo Placebo-controlled studies 0 en Placebo-controlled studies Post-hoc analysis 0 en Post-hoc analysis Post-randomized consent 0 en Post-randomized consent INST 102 en INST Subcategory of 102 en Subcategory of