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Human subject research
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#	Item
851	AIATSIS RESEARCH ETHICS COMMITTEE ETHICAL CLEARANCE PROPOSAL General Add to Reading List Source URL: www.aiatsis.gov.au Language: English - Date: 2014-06-17 01:30:45 Medical ethics Research Research ethics Design of experiments Pharmacology Informed consent Australian Institute of Aboriginal and Torres Strait Islander Studies Institutional review board Human subject research Applied ethics Ethics Clinical research
852	DEPARTMENT OF HEALTH & HUMAN SERVICES Office of the Secretary Office of Public Health and Science _________________________________________________________________________________________________ Add to Reading List Source URL: archive.hhs.gov Language: English - Date: 2010-03-22 18:57:29 Pharmacology Science Medical ethics Drug safety Design of experiments Institutional review board Office for Human Research Protections Food and Drug Administration Human subject research Clinical research Research Ethics
853	RESEARCH SUBJECTS INFORMATION UPDATED CUMC INSTITUTIONAL REVIEW BOARD (IRB) CONTACT INFORMATION The Columbia University Medical Center (CUMC) Institutional Review Board (IRB) is a committee that independently conducts on Add to Reading List Source URL: www.cumc.columbia.edu Language: English - Date: 2013-10-16 13:31:46 Medical ethics Applied ethics Design of experiments Pharmacology Drug safety Institutional review board Informed consent Human subject research Clinical research coordinator Clinical research Research Ethics
854	CCI #: _____________ ALBERT EINSTEIN COLLEGE OF MEDICINE OF YESHIVA UNIVERSITY COMMITTEE ON CLINICAL INVESTIGATIONS DRUG, DEVICE, AND GENE TRANSFER/GENE THERAPY HUMAN SUBJECT RESEARCH PROTOCOL APPLICATION Add to Reading List Source URL: archive.hhs.gov Language: English - Date: 2004-06-21 08:31:04 Health Pharmacology Pharmaceutical industry Food and Drug Administration Medical ethics Clinical trial Investigational New Drug Informed consent AECOM Research Medicine Clinical research
855	Ethics - Do I need ethics approval?   Add to Reading List Source URL: www.uregina.ca Language: English - Date: 2010-12-08 10:47:00 Clinical research Professional ethics Medical ethics Research ethics Confidentiality Debriefing Informed consent Human subject research Deception Ethics Applied ethics Behavior
856	Microsoft Word - Attachment 6.doc Add to Reading List Source URL: www.ryerson.ca Language: English - Date: 2011-06-30 14:48:02 Knowledge Disability Pharmaceutical industry Pharmacology Disability studies Clinical trial Catherine Frazee Inclusion Human subject research Health Science Clinical research
857	Instructions for Use of Form Add to Reading List Source URL: www.tn.gov Language: English - Date: 2008-06-04 12:58:49 Data privacy Privacy law Applied ethics Human subject research Health Insurance Portability and Accountability Act Pharmaceutical industry Institutional review board Clinical research Ethics Research
858	March 16, 2012 COLUMBIA UNIVERSITY INSTITUTIONAL REVIEW BOARD GUIDANCE STUDENTS AS RESEARCHERS I. SCOPE: Add to Reading List Source URL: cumc.columbia.edu Language: English - Date: 2013-01-08 12:22:18 Science Institutional review board Clinical trial Investigational New Drug Investigational Device Exemption Human subject research Ethics Committee Grant Health Insurance Portability and Accountability Act Clinical research Research Ethics
859	Microsoft Word - kronstadfinal Add to Reading List Source URL: archive.hhs.gov Language: English - Date: 2005-02-22 14:56:26 Applied ethics Human subject research Lana Skirboll United States Department of Health and Human Services Scientific method Belmont Report Clinical research Ethics Office for Human Research Protections
860	aprilminutes51506wotrack.doc Add to Reading List Source URL: www.epa.gov Language: English - Date: 2006-05-23 14:33:50 Applied ethics Research ethics Food Quality Protection Act Food law United States Environmental Protection Agency Aldicarb Ethyl carbamate Pesticide Human subject research Clinical research Ethics Research

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