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IRB: Ethics
Results: 397

#	Item
271	2009 IRB: Protocol Format Add to Reading List Source URL: www.uvawise.edu Language: English - Date: 2010-06-17 17:45:30 Science Design of experiments Pharmacology Medicine Drug safety Institutional review board Informed consent Communications protocol Clinical research coordinator Clinical research Medical ethics Research
272	University of Oklahoma IRB Add to Reading List Source URL: ouhsc.edu Language: English - Date: 2010-02-11 15:34:40 Medicine Ethics Design of experiments Pharmacology Medical research Institutional review board Belmont Report Public Responsibility in Medicine and Research National Commission for the Protection of Human Subjects of Biomedical and Behavioral Research Clinical research Medical ethics Research
273	Consent for Future Use of Specimens UH Biomedical IRB Consent for Future use of Biological Specimens Collected During this Research Project Add to Reading List Source URL: www.hawaii.edu Language: English - Date: 2014-05-23 21:49:15 Medical ethics Biological specimen Clinical research Biological databases Consent Department of Defense Serum Repository Institutional review board Ethics Biobanks Science
274	2009 IRB: Protocol Approval Form Page < PAGE >5 of < NUMPAGES >5 Add to Reading List Source URL: www.uvawise.edu Language: English - Date: 2010-06-17 17:45:20 Science Medical ethics Design of experiments Pharmacology Pharmaceutical industry Institutional review board Informed consent Human subject research Clinical research coordinator Clinical research Research Ethics
275	Institutional Review Board This document is designed to help you determine what you need to submit to the IRB in order to receive approval for your research. All research involving human participants conducted at UVA-Wi Add to Reading List Source URL: www.uvawise.edu Language: English - Date: 2010-06-17 17:45:52 Medicine Science Pharmaceutical industry Design of experiments Pharmacology Institutional review board Informed consent Clinical research coordinator Cooperative Human Tissue Network Clinical research Medical ethics Research
276	ABBOTT LABORATORIES Corporate Regulatory and Quality Science April Veoukas Corporate Regulatory Affairs D-3QC, AP6C-1 Add to Reading List Source URL: www.fda.gov Language: English - Date: 2004-10-21 10:34:55 Pharmaceutical sciences Science Design of experiments Medical ethics Drug safety Institutional review board Clinical trial Food and Drug Administration Certified IRB Professional Pharmacology Clinical research Research
277	Institutional Review Board North Dakota Department of Human Services Application for IRB Review of Research Involving the Use of Human Subjects Type all answers Add to Reading List Source URL: www.nd.gov Language: English - Date: 2008-02-22 15:17:54 Research Science Design of experiments Pharmacology Drug safety Institutional review board Informed consent Human subject research Belmont Report Clinical research Ethics Medical ethics
278	Rocky Mountain Tribal IRB COMMITTEE Rocky Mountain Tribal IRB COMMITTEE CONT. Behavioral Health Scientist Add to Reading List Source URL: www.mtwytlc.org Language: English - Date: 2011-07-06 12:03:56 Drug safety Institutional review board Ethics Scientific method Applied ethics Kutenai people Public Responsibility in Medicine and Research Clinical research Pharmacology Design of experiments
279	Microsoft Word - Decision Tree - Medical IRB Forms.doc Add to Reading List Source URL: www.nd.gov Language: English - Date: 2008-02-22 15:17:30 Research Informed consent Applied ethics Pharmaceutical industry Consent Institutional review board Clinical research coordinator Clinical research Medical ethics Ethics
280	Columbia University Medical Center Institutional Review Board FWA# [removed]IRB Registration or Sequence Number: IRB #4 (IRB00006882) Roster ID # Add to Reading List Source URL: www.columbia.edu Language: English - Date: 2013-08-06 16:17:05 Institutional review board Pharmacology Ethics Applied ethics Scientific method Clinical research Design of experiments Drug safety

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