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The top documents tagged [study endpoints]
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Compliance with the FDA Guidances on Investigator Responsibilities and the Form 1572
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ISAR-TEST-2 Trial Two-year Clinical and Angiographic Outcomes from a Randomized Trial of Polymer-Free Dual Drug-Eluting Stents versus Polymer-Based Cypher
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Building Quality into Clinical Trials and Avoiding Common Pitfalls Michael E. Marcarelli, PharmD Director, Division of Bioresearch Monitoring Office of
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FDA Final Rule & Revised NCI Guidelines for Expedited Reporting of Adverse Events S. Percy Ivy, MD Associate Chief, Senior Investigator Investigational
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Midterm results - Grades B to A+, mostly low A ethical theories14 rising health care costs7 23andme tests13 how are snps assayed4 GWAS6 critical eval of
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H. Awuoche 1, G.Kiringa 1, V. Nduba 1, E. Mitchell 2 1 KEMRI/CDC Research and Public Health Collaboration 2 KNCV Dutch Tuberculosis Foundation XIX International
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Health & Medicine
Mc Tiernan - 20th International Nutrition Congress 2013
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Eugm 2012 pritchett - application of adaptive sample size re-estimation in event outcome confirmatory trials - 2012 eugm
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Adaptive Design Methods in Clinical Trials Shein-Chung Chow, PhD Department of Biostatistics and Bioinformatics Duke University School of Medicine Durham,
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October 18, 2011 Device Development in Obesity and Metabolic Disease (DDOMD) Workshop Regulatory Considerations in Device Development Jonathan S. Kahan,
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Surrogate Endpoints: The Challenges are Greater than they Seem March 7, 2005 Thomas R. Fleming, Ph.D. Professor and Chair of Biostatistics University of
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A Phase II Study of Lenalidomide as Initial Treatment of Elderly Patients with Chronic Lymphocytic Leukemia Xavier Badoux, William Wierda, Susan O'Brien,
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