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IRB: Ethics
Results: 397

#	Item
291	4734560247650Approval Date: 00Approval Date: [removed]190500For IRB Use Only 00For IRB Use Only[removed] Add to Reading List Source URL: research.unt.edu Language: English - Date: 2013-09-03 09:56:44 Research Design of experiments Pharmacology Behavior Drug safety Institutional review board Email Psychology Informed consent Clinical research Medical ethics Science
292	Microsoft Word - Start_a_TCU_or_Tribal_IRB.doc Add to Reading List Source URL: depts.washington.edu Language: English - Date: 2007-06-13 12:16:46 Medical ethics Design of experiments Science Scientific method Drug safety Institutional review board Office for Human Research Protections Public Responsibility in Medicine and Research Cooperative Human Tissue Network Clinical research Research Pharmacology
293	Columbia University IRB Policy Data Security Plans Involving the Use, Storage or Transmission of Electronic Research Data Constituting Sensitive Data I. Background Add to Reading List Source URL: www.columbia.edu Language: English - Date: 2013-11-18 10:33:00 Computer security Law Data security Privacy law Computer law Information security Personally identifiable information Health Insurance Portability and Accountability Act Payment Card Industry Data Security Standard Data privacy Security Ethics
294	IRB SOPs Version 4.2 Nov. 2, 2012 Table of Contents SOP Cover Page Introduction to the Columbia Human Research Protection Program Institutional Leadership Institutional Culture Standard Operating Procedures Add to Reading List Source URL: www.columbia.edu Language: English - Date: 2012-11-19 12:30:23 Science Design of experiments Pharmacology Medical ethics Drug safety Institutional review board Clinical trial Investigational New Drug Public Responsibility in Medicine and Research Clinical research Research Medicine
295	IRB BASIC TRAINING ON THE PROTECTION OF HUMAN PARTICIPANTS IN RESEARCH Add to Reading List Source URL: www.columbia.edu Language: English - Date: 2006-02-03 18:37:56 Research Drug safety Institutional review board Scientific method Ethics Columbia University Recruit training Clinical research Design of experiments Pharmacology
296	Guidance on IRB Meeting Minutes Add to Reading List Source URL: www.compliance.iastate.edu Language: English - Date: 2009-07-01 10:34:44 Research Scientific method Design of experiments Pharmacology Pharmaceutical industry Institutional review board Informed consent Minutes Adverse event Clinical research Ethics Medical ethics
297	NUHS Guidance for Case Studies This guidance is intended to assist an investigator preparing a case report to determine if a study is research that requires IRB review. Completed Guidance should be submitted to the NUHS Add to Reading List Source URL: www.nuhs.edu Language: English - Date: 2014-03-06 10:37:03 Medicine Health Pharmaceutical industry Design of experiments Pharmacology Institutional review board Clinical research coordinator Informed consent Medical record Clinical research Research Medical ethics
298	[removed]4191000247650Approval Date: 00Approval Date: [removed]190500For IRB Use Only 00For IRB Use Only Add to Reading List Source URL: research.unt.edu Language: English - Date: 2014-06-18 17:00:01 Medicine Medical ethics Design of experiments Pharmacology Drug safety Institutional review board Human subject research National Institutes of Health Informed consent Clinical research Research Ethics
299	4734560247650Approval Date: 00Approval Date: [removed]190500For IRB Use Only 00For IRB Use Only[removed] Add to Reading List Source URL: research.unt.edu Language: English - Date: 2013-09-03 09:56:11 Science Design of experiments Pharmacology Drug safety Scientific method Institutional review board University of North Texas Informed consent Email Clinical research Medical ethics Research
300	4734560247650Approval Date: 00Approval Date: [removed]190500For IRB Use Only 00For IRB Use Only[removed] Add to Reading List Source URL: research.unt.edu Language: English - Date: 2013-09-03 09:55:33 Pharmacology Research Drug safety Applied ethics Science Institutional review board Informed consent University of North Texas Clinical research coordinator Clinical research Medical ethics Design of experiments

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