Digitale Bibliotheek
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                             173 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 A09 A data coordinating center model for expanded access clinical trials Yucaitis, Joy
1993
14 5 p. 402-
1 p.
artikel
2 A26 A functional paradigm for clinical trial design Greenfield, Mary Lou
1993
14 5 p. 409-
1 p.
artikel
3 A65 A methodology to perform the “paperless” clinical trial: Electronic signatures for electronic data Bailey, Lance R.
1993
14 5 p. 425-426
2 p.
artikel
4 A64 A methodology to perform the “paperless” clinical trial: Overview and general principles Rochon, James
1993
14 5 p. 425-
1 p.
artikel
5 A36 Analysis of long term adverse experience data using the Weibull model Shapiro, Deborah R.
1993
14 5 p. 413-
1 p.
artikel
6 A16 An assessment of the value of double data entry and interactive checking Fabri, Jackie
1993
14 5 p. 405-
1 p.
artikel
7 A66 An integrated clinical trial database integrity evaluation system (DIES) Levinson, Mark A.
1993
14 5 p. 426-
1 p.
artikel
8 A18 A simulation study of the number of events per variable recommended in multivariable regression analyses Peduzzi, Peter
1993
14 5 p. 406-
1 p.
artikel
9 A17 A statistical design for multivariate study end-points Luo, X.
1993
14 5 p. 406-
1 p.
artikel
10 A13 Automated data entry using fax with optical character recognition Achtenberg, Joel
1993
14 5 p. 404-
1 p.
artikel
11 A48 Balancing treatment assignments in trials with large number of centers Colopy, Mike
1993
14 5 p. 418-
1 p.
artikel
12 A27 Beta errors revisited Moher, D.
1993
14 5 p. 410-
1 p.
artikel
13 A06 Changing the study design during the recruitment phase of an international perinatal multicentre clinical trial Weston, Julie
1993
14 5 p. 401-
1 p.
artikel
14 A19 Classification and regression trees as a tool to identify prognostic factors in long-term clinical trials Hasford, J.
1993
14 5 p. 406-407
2 p.
artikel
15 A63 Collection of electronic clinical data from UK community doctors Bourke, Alison
1993
14 5 p. 425-
1 p.
artikel
16 A35 Comparison of analytical methods when response fluctuates between success and failure Linton, Kathryn L.P.
1993
14 5 p. 413-
1 p.
artikel
17 A30 Computerized and centralized participant entry in large-scale, multi-centered clinical trials Cronin, Walter M.
1993
14 5 p. 411-
1 p.
artikel
18 A02 Confidence intervals for power probabilities: How powerful was that hypothesis test? O'Brien, Ralph G.
1993
14 5 p. 399-
1 p.
artikel
19 A38 Confidence intervals for the median survival time adjusted for covariates Karrison, Theodore
1993
14 5 p. 414-
1 p.
artikel
20 A25 Cooperative clinical trials in health services research in the department of veterans affairs Henderson, William G.
1993
14 5 p. 409-
1 p.
artikel
21 A07 Data management workload assessment for medical oncology Trochanowski, B.
1993
14 5 p. 401-402
2 p.
artikel
22 A15 Data quality assurance in a distributed data entry environment: An alternative to 100% keystroke verification Clayton, K.J.
1993
14 5 p. 405-
1 p.
artikel
23 A24 Design considerations in community based randomized trials Gordon, Mae E.
1993
14 5 p. 408-409
2 p.
artikel
24 A50 Development of a new instrument: Quality of life in epilepsy (QOLIE) Creamer, Joyce
1993
14 5 p. 419-
1 p.
artikel
25 A59 Development of a software using a touch tone phone system and a vocal interface for automatic registration and randomization in multicenter clinical trials: Further experience of the European lung cancer working party Paesmans, M.
1993
14 5 p. 423-
1 p.
artikel
26 A54 Does a placebo run-in identify poor adherers?: An empirical evaluation in the cholesterol reduction in seniors Davis, C.E.
1993
14 5 p. 421-
1 p.
artikel
27 A22 Drug development issues in the pacific region: Cost-effectiveness Defina, John A.
1993
14 5 p. 407-408
2 p.
artikel
28 A23 Economic implications of results from a clinical trial Fink, Nancy
1993
14 5 p. 408-
1 p.
artikel
29 A60 Ethics and statistical methodology in clinical trials Palmer, Christopher R.
1993
14 5 p. 423-
1 p.
artikel
30 A04 Evaluating noninvasive monitoring outside the intensive care unit: A method to enhance the before-after trial Inman, K.J.
1993
14 5 p. 400-
1 p.
artikel
31 A37 Exact logistic regression for small-sample clustered binary data Mehta, Cyrus R.
1993
14 5 p. 414-
1 p.
artikel
32 A34 Factor analytic strategies for evaluating generalizability of construct validity Cornell, John E.
1993
14 5 p. 413-
1 p.
artikel
33 A53 Factors predicting employment and job satisfaction in patients with severe left ventricular dysfunction Ahn, Sylvie
1993
14 5 p. 420-
1 p.
artikel
34 A57 Further experience with a 24-hour-a-day computerized randomization service Weston, Julie
1993
14 5 p. 422-
1 p.
artikel
35 A33 Identifying successful recruitment strategies in the lipid trial Hague, W.
1993
14 5 p. 412-
1 p.
artikel
36 A45 Interim analysis methods in the colon cancer control study Church, Timothy
1993
14 5 p. 417-
1 p.
artikel
37 A14 Lack of added-value from double data entry Day, Simon
1993
14 5 p. 404-405
2 p.
artikel
38 A41 Logistics of closeout in the asymptomatic carotid artery plaque study (ACAPS) Margitić, Susan E.
1993
14 5 p. 415-
1 p.
artikel
39 A43 Long-term survival follow-up in international clinical trials Haugh, Margaret C.
1993
14 5 p. 416-
1 p.
artikel
40 A58 Maintaining the integrity of a long-term randomized controlled trial using school districts as the unit of randomization Mann, Sue
1993
14 5 p. 422-423
2 p.
artikel
41 A46 On closed test procedures for dose response analysis Rom, Dror M.
1993
14 5 p. 417-
1 p.
artikel
42 A29 Optimizing patient selection in therapeutic experiments Moons, K.G.M.
1993
14 5 p. 410-411
2 p.
artikel
43 A01 Power analysis of cutoff-based randomized clinical trials C. Cappelleri, Joseph
1993
14 5 p. 399-
1 p.
artikel
44 A03 Powerspending in clinical trials using alpha-spending stopping rules van Rossum, Jim
1993
14 5 p. 400-
1 p.
artikel
45 A21 Principles of agreement for post NDA clinical trials Holbrook, Janet T.
1993
14 5 p. 407-
1 p.
artikel
46 A56 Randomization and treatment assignment in the CPCRA Connett, John
1993
14 5 p. 422-
1 p.
artikel
47 A55 Randomization in the APOLO study: A necessary compromise between the study design and practical constraints Boissel, Jean-Pierre
1993
14 5 p. 421-
1 p.
artikel
48 A44 Reducing patient withdrawals in a large multi-center clinical trial Lee, Jennifer
1993
14 5 p. 416-417
2 p.
artikel
49 A49 Reporting of allocation methods in clinical trials Williams, Diane H.
1993
14 5 p. 418-419
2 p.
artikel
50 A31 Representation of women and minorities in published clinical trials Duffy, Barbara A.
1993
14 5 p. 411-
1 p.
artikel
51 A61 Sample size and monitoring criteria for Bayesian phase II clinical trials Thall, Peter F.
1993
14 5 p. 424-
1 p.
artikel
52 A62 Sample size re-estimation in response to treatment noncompliance Cosmatos, Dennis
1993
14 5 p. 424-
1 p.
artikel
53 A08 Self-administered quality of life forms: Experience from the post coronary artery bypass graft studies Fox, Norma Lynn
1993
14 5 p. 402-
1 p.
artikel
54 A28 Should there be restrictions on indicator lesions for phase II trials in oncology? Franklin, Hilary
1993
14 5 p. 410-
1 p.
artikel
55 A32 Simultaneous patient enrollment in multiple randomized trials: Experience in GUSTO Granger, Christopher
1993
14 5 p. 412-
1 p.
artikel
56 A47 Statistical treatment comparisons for a trial of thrombolytic therapy in acute myocardial infarction Lee, Kerry L.
1993
14 5 p. 418-
1 p.
artikel
57 A51 The clinical and economic impact of clozapine treatment of refractory schizophrenia Rosenheck, Robert
1993
14 5 p. 419-
1 p.
artikel
58 A39 The GUSTO large trial experience with designing inservice materials Huffman, Caroline M.
1993
14 5 p. 414-415
2 p.
artikel
59 A42 The publications and presentations committee: What makes it work? Margitić, Susan E.
1993
14 5 p. 416-
1 p.
artikel
60 A40 The use of a non-compliance index to predict the feasibility of clinical trials De Rosa, M.
1993
14 5 p. 415-
1 p.
artikel
61 A52 The use of echocardiography in multicenter trials: Experience from the treatment of mild hypertension study (TOMHS) Granditis, Greg A.
1993
14 5 p. 420-
1 p.
artikel
62 A05 Use of a sequential method for monitoring safety in patients enrolled in the multicenter acute stroke trial Boutitie, F.
1993
14 5 p. 401-
1 p.
artikel
63 A20 Validation of surrogate outcomes for evaluation of cancer screening intervention Barlow, William E.
1993
14 5 p. 407-
1 p.
artikel
64 Design and methods of a clinical trial for a rare condition: The collaborative ocular melanoma study 1993
14 5 p. 362-391
30 p.
artikel
65 Fifteenth annual meeting of the society for clinical trials 1993
14 5 p. 392-
1 p.
artikel
66 P76 A computerized drug distribution system for a multicenter, international clinical trial Christopher, Donna L.
1993
14 5 p. 459-
1 p.
artikel
67 P10 A computerized network system for the management of a large scale multicentre clinical trial: The GISSI-3 trial Santoro, Eugenio
1993
14 5 p. 430-
1 p.
artikel
68 P52 A computerized patient-donor tracking system to facilitate marrow transplants Randall, Bryan L.
1993
14 5 p. 448-449
2 p.
artikel
69 P71 Adverse event reporting in an AIDS trial Isaacson, Milana
1993
14 5 p. 457-
1 p.
artikel
70 P89 A generalized log-logistic model for analysis of interval-censored failure time data Singh, Karan P.
1993
14 5 p. 465-
1 p.
artikel
71 P39 A meta-analysis in preventing restenosis after percutaneous transluminal coronary angioplasty Huang, David C.
1993
14 5 p. 443-
1 p.
artikel
72 P48 Analysis of ratios: A case study based on arterial distensibility Evans, G.W.
1993
14 5 p. 447-
1 p.
artikel
73 P61 An automated telephone response system Pollizzi, S.
1993
14 5 p. 452-
1 p.
artikel
74 P59 A quality assurance program in cancer clinical trials Niland, Joyce
1993
14 5 p. 451-452
2 p.
artikel
75 P51 Archiving and material storage for a long-term clinical trial Coates, Townes C.
1993
14 5 p. 448-
1 p.
artikel
76 P53 A self-report design promoting the validity and re retrieval rate outcome measures in a controlled trial of dichlorphenamide in periodic paralysis Herr, Barbara
1993
14 5 p. 449-
1 p.
artikel
77 P49 A simple trial? Jevons, Caroline M.
1993
14 5 p. 447-
1 p.
artikel
78 P57 BMDPLOT: Publication-quality survival plots from BMDP output Corley, S.
1993
14 5 p. 451-
1 p.
artikel
79 P13 Centralized control of an automated telephone response system Mirenzi, Evelyn
1993
14 5 p. 432-
1 p.
artikel
80 P43 Clinical panel assessment of photodamaged skin treated with isotretinoin using photographs Armstrong, Robert B.
1993
14 5 p. 445-
1 p.
artikel
81 P58 Cluster sampling to estimate key entry error rates Pearce, Lesly A.
1993
14 5 p. 451-
1 p.
artikel
82 P32 Collecting quality of life (QOL) information: Does it facilitate or impede physician accrual of eligible patients to randomized cancer trials? Taylor, Kathryn M.
1993
14 5 p. 440-
1 p.
artikel
83 P75 Complexities of altering the study design of a large clinical trial in progress without interrupting enrollment Christopher, Donna L.
1993
14 5 p. 458-459
2 p.
artikel
84 P14 Computer generated electronic mail in clinical trials Turner, Martha W.
1993
14 5 p. 432-
1 p.
artikel
85 P65 Considerations for a group sequential, dose-response trial design Anderson, Keaven M.
1993
14 5 p. 454-
1 p.
artikel
86 P68 Constructing confidence intervals about multiple indices of effect size Borenstein, Michael
1993
14 5 p. 455-
1 p.
artikel
87 P77 Coordinating drug distribution for a large clinical trial Christopher, Donna L.
1993
14 5 p. 459-
1 p.
artikel
88 P87 Coping with the fast change of medical technology in clinical trials Binkowitz, Bruce S.
1993
14 5 p. 464-
1 p.
artikel
89 P85 Cox regression versus discriminant techniques: Can we predict a high risk group in stage I epithelial ovarian cancer? Dunn, Janet A.
1993
14 5 p. 463-
1 p.
artikel
90 P03 Creating archival tapes for sharing final study data Raiz, Pauline
1993
14 5 p. 427-
1 p.
artikel
91 P09 Database management of national cancer institute-sponsored cancer treatment trials Phillips, Pamela H.
1993
14 5 p. 430-
1 p.
artikel
92 P27 Data monitoring issues in cancer screening trials Wells, Barbara L.
1993
14 5 p. 438-
1 p.
artikel
93 P55 Designing a registration system for the clinical research database system Pan, Q.
1993
14 5 p. 450-
1 p.
artikel
94 P63 Design of a randomized trial of combined nucleoside analog antiretroviral therapy in AIDS patients Church, Timothy
1993
14 5 p. 453-
1 p.
artikel
95 P18 Development of a monitor driven clinical grant payment tracking and forecasting information system Nonomura, John
1993
14 5 p. 434-
1 p.
artikel
96 P47 Development of an historical control series in assessing treatment effect of instrumenting spine disorders Carlow, John J.
1993
14 5 p. 446-
1 p.
artikel
97 P88 Deviation of actual longitudinal data collection times from “ideal” times Keller, Jean A.
1993
14 5 p. 464-465
2 p.
artikel
98 P54 Educating data managers — What needs to be done? Quinlivan, S.
1993
14 5 p. 449-450
2 p.
artikel
99 P01 Educational activities of the Dutch working group for data managers Boon, Mildred C.
1993
14 5 p. 426-
1 p.
artikel
100 P19 Efficacy/compliance relationship in a large scale trial on hypertensive patients Boissel, Jean-Pierre
1993
14 5 p. 434-
1 p.
artikel
101 P82 Efficacy of double-blinding in a randomized controlled trial (RCT) of low dose warfarin to prevent thromboembolic disease in patients with metastatic breast cancer Dickson, Lenore
1993
14 5 p. 462-
1 p.
artikel
102 P41 Equivalence testing using available statistical software Alvir, Jose Ma.J.
1993
14 5 p. 444-
1 p.
artikel
103 P04 Establishment of an adverse event reporting (AER) database: The National Cancer Institute of Canada clinical trials group (NCIC CTG) experience Muldal, A.
1993
14 5 p. 428-
1 p.
artikel
104 P86 Evaluating the strength of prognostic factors in a series of 1400 patients with myelomatosis Dunn, Janet A.
1993
14 5 p. 464-
1 p.
artikel
105 P02 Experience with geographically-distributed data entry in multi-center clinical trials Gee, Lauren
1993
14 5 p. 427-
1 p.
artikel
106 P66 Factors influencing women's clinical trial participation Valanis, Barbara G.
1993
14 5 p. 455-
1 p.
artikel
107 P79 Global coordination of a 41,000 patient international trial Karnash, Sharon
1993
14 5 p. 460-461
2 p.
artikel
108 P78 Hotline calls: A key to communication in a large trial Davis, Catherine
1993
14 5 p. 460-
1 p.
artikel
109 P26 Improving patient compliance Baker, Patricia G.
1993
14 5 p. 437-
1 p.
artikel
110 P64 Instrument development: Rolls-Royce versus Volkswagen Rush, B.
1993
14 5 p. 454-
1 p.
artikel
111 P60 Interfacing microsoft excel 4.0® and SAS® for report generation in clinical trials Goodwin, Robert R.
1993
14 5 p. 452-
1 p.
artikel
112 Plenary session III- Brother, can you sponsor a trial? The story of the survival and ventricular enlargement study (SAVE) 1993
14 5 p. 398-
1 p.
artikel
113 Plenary session II- Intention to treat — New issues 1993
14 5 p. 395-
1 p.
artikel
114 Plenary session I - Outcomes research —The role of randomized clinical trial 1993
14 5 p. 394-
1 p.
artikel
115 P22 Linking protocol to forms development through the use of a relational database in multi-disciplinary randomized clinical trials Edwards, Carol
1993
14 5 p. 435-436
2 p.
artikel
116 P34 Methods of outcome assessment in National Eye Institute sponsored multicenter clinical trials McCaffrey, Lee
1993
14 5 p. 441-
1 p.
artikel
117 P38 Methods of school-based data collection in longitudinal prevention trials Renshaw-Myrwang, Renée
1993
14 5 p. 443-
1 p.
artikel
118 P45 Modeling the time dependency of circulating microbubbles on symptoms of decompression sickness for space extravehicular activities Kumar, K.Vasantha
1993
14 5 p. 445-446
2 p.
artikel
119 P07 Monitoring completion of data form discrepancies Pelusio, Rita M.
1993
14 5 p. 429-
1 p.
artikel
120 P20 Monitoring safety in a multi-center clinical trial of acute ischemic stroke Clarke, William R.
1993
14 5 p. 435-
1 p.
artikel
121 P81 No more lost to follow-up! insuring complete patient tracking post hospital discharge: The caveat coordinating center experience Berdan, Lisa G.
1993
14 5 p. 461-462
2 p.
artikel
122 P25 Outcome assessment in the treatment of acute low back pain Malmivaara, Antti
1993
14 5 p. 437-
1 p.
artikel
123 P12 Patient accrual: Past experience, future options Ward, Linda
1993
14 5 p. 431-
1 p.
artikel
124 P74 Personalizing a large trial: Every sites' contribution counts Smith, Deborah D.
1993
14 5 p. 458-
1 p.
artikel
125 P35 Phantom or real? Verification of nonrandomized patients evaluated for randomized clinical trials for a rare disease Manos, Kelly S.
1993
14 5 p. 441-
1 p.
artikel
126 P15 Phase IV clinical trials: The good, the bad, and the ugly Decoster, Genevieve
1993
14 5 p. 432-433
2 p.
artikel
127 P05 Phases of data form design for the obstetrical triage study Meininger, Elise
1993
14 5 p. 428-
1 p.
artikel
128 P90 Pooling data from five stroke prevention clinical trials versus performing a meta-analysis Fletcher, K.A.
1993
14 5 p. 465-
1 p.
artikel
129 P62 Preditor: An organized and efficient approach for ensuring data quality in a clinical trial Martin, Jeffrey
1993
14 5 p. 453-
1 p.
artikel
130 P50 Project control of software applications Karabelas, Susan
1993
14 5 p. 448-
1 p.
artikel
131 P28 Promoting enrollment in a multi-center clinical trial Rudolph, Alice
1993
14 5 p. 438-
1 p.
artikel
132 P08 Providing stable data structures for interim analysis of a growing database Eng, Heather
1993
14 5 p. 429-
1 p.
artikel
133 Preconference workshop 2 overview of good clinical practices! FDA Audits — How to avoid the common pitfalls 1993
14 5 p. 393-
1 p.
artikel
134 Preconference workshop 1 the development and evolution of funded clinical trial initiatives 1993
14 5 p. 393-
1 p.
artikel
135 P29 Recruitment of breast cancer patients to clinical trials: General issues and barriers Siminoff, Laura A.
1993
14 5 p. 438-439
2 p.
artikel
136 P33 Recruitment strategies in rheumatoid arthritis (RA) clinical trials (CT): The mira experience Tilley, Barbara C.
1993
14 5 p. 440-
1 p.
artikel
137 P36 Responses to ethical and other questions on a knowledge assessment form for a multicenter trial Scherer, R.
1993
14 5 p. 442-
1 p.
artikel
138 P24 Role of site and central laboratories in multi-center clinical trials: An illustration from a VA cooperative infectious disease trial Voynick, Irene M.
1993
14 5 p. 436-
1 p.
artikel
139 P31 Salvaging clinical trials forced to terminate early by results of external information Zee, B.
1993
14 5 p. 439-440
2 p.
artikel
140 P21 Selecting and monitoring alert levels — What are the issues? Wasilauskas, Carol H.
1993
14 5 p. 435-
1 p.
artikel
141 P30 Selection of quality of life instruments for the MDRD study and results of baseline analyses Gassman, Jennifer
1993
14 5 p. 439-
1 p.
artikel
142 P67 Sensitivity of power computations for design considerations in clinical trials Arena, Vincent C.
1993
14 5 p. 455-
1 p.
artikel
143 P23 Shift tables for presentation of clinical data Bristol, David R.
1993
14 5 p. 436-
1 p.
artikel
144 P80 Source verification in large clinical trials: Is 10% enough? Karnash, Sharon
1993
14 5 p. 461-
1 p.
artikel
145 P70 Stage migration in a surgical trial Bunt, A.M.G.
1993
14 5 p. 456-
1 p.
artikel
146 P69 Standardization in a surgical trial Bunt, A.M.G.
1993
14 5 p. 456-
1 p.
artikel
147 P73 Standardizing documentation for trials Van Natta, Mark
1993
14 5 p. 457-458
2 p.
artikel
148 P37 Starting research in new areas: Health care directives in the institutionalized elderly Urbanyi, Mafalda
1993
14 5 p. 442-
1 p.
artikel
149 P84 Statistical analysis of coronary angiographic data: patients or lesions? Mack, Wendy J.
1993
14 5 p. 463-
1 p.
artikel
150 P44 Statistical issues in the design and analysis of clinical trials evaluating therapy for chronic asthma Ji Zhang,
1993
14 5 p. 445-
1 p.
artikel
151 P16 Statistical issues in the design of the trial of nonpharmacologic interventions in the elderly (tone) Espeland, Mark
1993
14 5 p. 433-
1 p.
artikel
152 P17 Summarizing carotid intimal-medial thickness in the asymptomatic carotid artery plaque study Hoen, Helena
1993
14 5 p. 433-
1 p.
artikel
153 P83 Survival analysis of 4-period, 4-treatment crossover design with repeated measures Chao Wang,
1993
14 5 p. 462-
1 p.
artikel
154 P11 System for monitoring timing of data review and entry Zee, Benny
1993
14 5 p. 431-
1 p.
artikel
155 P06 Taking control of your clinical trial: Remote database management (RDM) Rushing, Scott
1993
14 5 p. 428-429
2 p.
artikel
156 P42 The effect of drug exposure on incidence rates of adverse clinical events within antibiotic trials Rutkiewicz, Victoria
1993
14 5 p. 444-445
2 p.
artikel
157 P40 The identification of prognostic factors in breast cancer Ulm, K.
1993
14 5 p. 443-444
2 p.
artikel
158 P72 Therapy adherence and mortality in the cardiac arrhythmia suppression trial Manno, Dulce Obias
1993
14 5 p. 457-
1 p.
artikel
159 P46 Two randomized equivalence trials in pediatric oncology: Analysis of censored data Com-Nougue, C.
1993
14 5 p. 446-
1 p.
artikel
160 P56 Using data management statistics and system resources statistics for quality assurance Remaley, Nancy H.
1993
14 5 p. 450-451
2 p.
artikel
161 S11 Estimating the treatment effect on survival from right-censored data in a randomized clinical trial with non-random noncompliance Hu, Fu-Chung
1993
14 5 p. 403-
1 p.
artikel
162 S12 Lower confidence bounds for time to cure Rabinowitz, Daniel
1993
14 5 p. 404-
1 p.
artikel
163 S10 Planning of clinical trials using biomarkers as endpoints Kirby, Alison J.
1993
14 5 p. 403-
1 p.
artikel
164 Statistical considerations in monitoring the Systolic Hypertension in the Elderly Program (SHEP) Davis, Barry R.
1993
14 5 p. 350-361
12 p.
artikel
165 Suspended judgment from “tame” to “forbidden” death Silverman, William A.
1993
14 5 p. 347-349
3 p.
artikel
166 Workshop II- Data management issues related to preparation and release of study data 1993
14 5 p. 394-
1 p.
artikel
167 Workshop III- Consumers and their influence on the design and conduct of clinical trials 1993
14 5 p. 395-
1 p.
artikel
168 Workshop I- The use of health-related quality of life measures in cross national clinical trials. Issues and perspectives 1993
14 5 p. 394-
1 p.
artikel
169 Workshop IV- Partnership opportunities among academia, venture capitalists, contract research organizations, and industry 1993
14 5 p. 396-
1 p.
artikel
170 Workshop V- Adapting generic quality of life scales to specific populations 1993
14 5 p. 396-
1 p.
artikel
171 Workshop VIII- Recruitment issues in research: A focus on women and minorities 1993
14 5 p. 398-
1 p.
artikel
172 Workshop VII- Issues in analyzing disease progression using clinical classification systems 1993
14 5 p. 397-
1 p.
artikel
173 Workshop VI- New technologies in data capture 1993
14 5 p. 397-
1 p.
artikel
                             173 gevonden resultaten
 
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