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The top documents tagged [welfare of human subjects]
Patricia S. Kerby, MPA Office of Human Subjects Protection January 7, 2009 How to Survive an FDA Inspection
213 views
Human Subjects Research created April, 2009. RCR – Human Subjects RCR – Human Subjects Short pre-test Presentation Objectives NIH Comment background regulation,
221 views
Drawing the Lines – Determining What Needs IRB Review 2009 VA Chair IRB Meeting October 7-8, 2009 Bethesda, MD Michael A. Carome, M.D. CAPT, U.S. Public
212 views
Clinical Trial Process: Overview
6.909 views
Kusum Verma A.I.I.M.S. New Delhi. WHY - CONCERN Research essential for advancement of scientific knowledge. Newer technologies & treatments. Require participation
217 views
Institutional Review Board Protecting Human Subjects in Research Presented by: Kathleen E. Furr Asst. Director of Research Administration PAC 515, 217.206.7409
218 views
Ethical Oversight of Human Subject Research Funding was provided through a Community Engagement Supplement to the Oregon Clinical and Translational Research
214 views
UH employees and students who conduct research involving human subjects are required to obtain approval from the Committee on Human Studies (CHS). John
213 views
University of Indianapolis Institutional Review Board Protecting Study Volunteers in Research
213 views
INSTITUTIONAL REVIEW OF RESEARCH INVOLVING HUMAN PARTICIPANTS IRB PRESENTATION UNIVERSITY OF CENTRAL FLORIDA OFFICE OF RESEARCH & COMMERCIALIZATION 407-823-2901
216 views
Presented by The Research Integrity Office. Knowledgeable ▪ The regulations, research, the IRB process Thorough Thoughtful Collaborative ▪ With
215 views
Multisite Studies: Communication Among IRBs, Investigators, and Sponsors Marisue Cody, PhD Deputy Director, PRIDE
216 views
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