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
Documents Patricia S. Kerby, MPA Office of Human Subjects Protection January 7, 2009 How to Survive an FDA Inspection

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Human Subjects Research created April, 2009. RCR – Human Subjects RCR – Human Subjects Short pre-test Presentation Objectives NIH Comment background regulation,
Documents Human Subjects Research created April, 2009. RCR – Human Subjects RCR – Human Subjects Short pre-test Presentation Objectives NIH Comment background regulation,

223 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
Documents 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

213 views

Clinical Trial Process: Overview
Business Clinical Trial Process: Overview

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Kusum Verma A.I.I.M.S. New Delhi. WHY - CONCERN Research essential for advancement of scientific knowledge. Newer technologies & treatments. Require participation
Documents Kusum Verma A.I.I.M.S. New Delhi. WHY - CONCERN Research essential for advancement of scientific knowledge. Newer technologies & treatments. Require participation

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Institutional Review Board Protecting Human Subjects in Research Presented by: Kathleen E. Furr Asst. Director of Research Administration PAC 515, 217.206.7409
Documents Institutional Review Board Protecting Human Subjects in Research Presented by: Kathleen E. Furr Asst. Director of Research Administration PAC 515, 217.206.7409

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Ethical Oversight of Human Subject Research Funding was provided through a Community Engagement Supplement to the Oregon Clinical and Translational Research
Documents Ethical Oversight of Human Subject Research Funding was provided through a Community Engagement Supplement to the Oregon Clinical and Translational Research

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UH employees and students who conduct research involving human subjects are required to obtain approval from the Committee on Human Studies (CHS). John
Documents UH employees and students who conduct research involving human subjects are required to obtain approval from the Committee on Human Studies (CHS). John

214 views

University of Indianapolis Institutional Review Board Protecting Study Volunteers in Research
Documents University of Indianapolis Institutional Review Board Protecting Study Volunteers in Research

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INSTITUTIONAL REVIEW OF RESEARCH INVOLVING HUMAN PARTICIPANTS IRB PRESENTATION UNIVERSITY OF CENTRAL FLORIDA OFFICE OF RESEARCH & COMMERCIALIZATION 407-823-2901
Documents INSTITUTIONAL REVIEW OF RESEARCH INVOLVING HUMAN PARTICIPANTS IRB PRESENTATION UNIVERSITY OF CENTRAL FLORIDA OFFICE OF RESEARCH & COMMERCIALIZATION 407-823-2901

217 views

Presented by The Research Integrity Office. Knowledgeable ▪ The regulations, research, the IRB process Thorough Thoughtful Collaborative ▪ With
Documents 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
Documents Multisite Studies: Communication Among IRBs, Investigators, and Sponsors Marisue Cody, PhD Deputy Director, PRIDE

217 views