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The top documents tagged [elements of informed]
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FDA Compliance Actions Against IRBs and Clinical Investigators Paul W. Goebel, Jr., CIP Vice President
[email protected]
Chesapeake Research Review,
217 views
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Wendy Lloyd BA, LPN, CIP,CCRP Regulatory Affairs and Compliance Specialist
224 views
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Informed Consent Philosophy 2803 Lecture IV Feb. 5, 2003
213 views
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BUILDING INFORMED CONSENT FOR PESTICIDE HANDLERS IN WASHINGTON Karl F. Weyrauch MD MPH Family Physician Research Consultant UW PNASH Member, Western Institutional
218 views
Health & Medicine
Informed consent
397 views
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1 Choice and Autonomy Ethical Issues in Women’s Health Meredith Schwartz Dalhousie University, Department of Philosophy
212 views
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Northeast Ethics Education Partnership (NEEP) Training Resources To access NEEP’s training materials, please visit
230 views
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Ethical Principles for Biomedical Research Involving Human Subjects: Overview of International Guidelines Maria Fidelis C. Manalo, MD, MSc Epidemiology
222 views
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Use of a Short Form For inclusion of non-English speaking participants in human subject research * To play the presentation, click on the icon on the
216 views
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Using the short form and reporting adverse events Erin Coons, Senior IRB Specialist, COMIRB 1
216 views
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Institutional Review Board (IRB) Human Subject Dr. John N. Austin, Director and Ms. Renee S. Jones, Associate Director Delaware State University Office
216 views
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Institutional Review Board (IRB) Human Subject Delaware State University Office of Sponsored Programs
219 views
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