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Human subject research
Results: 1674

#	Item
761	Chadron State College Institutional Review Board IRB Full Board Review Application Form Submit one original copy with signatures and one digital copy, with signatures, IRB Administrative Chair—allow at least four w Add to Reading List Source URL: www.csc.edu Language: English - Date: 2012-11-09 22:46:27 Medical ethics Applied ethics Research ethics Design of experiments Pharmacology Institutional review board Informed consent Human subject research Psychology Clinical research Ethics Research
762	Chadron State College Institutional Review Board Request for Administratively-Reviewed Exempt Certification Submit one complete copy to IRB Administrative Chair – allow at least two weeks for review Research Project T Add to Reading List Source URL: www.csc.edu Language: English - Date: 2012-11-09 22:46:18 Medical ethics Research Research ethics Design of experiments Pharmacology Institutional review board Informed consent Human subject research Clinical research coordinator Clinical research Ethics Applied ethics
763	Cost Sharing on Extramural Sponsored Projects Add to Reading List Source URL: www.research.uci.edu Language: English - Date: 2014-02-06 19:16:06 Scientific method Institutional review board Institutional Animal Care and Use Committee Public Responsibility in Medicine and Research Adverse event Grant National Institutes of Health Animal testing Human subject research Clinical research Research Science
764	The University of Connecticut Health Center INSTITUTIONAL REVIEW BOARD Request for Exemption Add to Reading List Source URL: hspo.uchc.edu Language: English - Date: 2014-03-28 11:05:26 Applied ethics Design of experiments Pharmacology Medical ethics Drug safety Institutional review board Human subject research Guidelines for human subject research Clinical research Ethics Research
765	Missouri Southern State University Human Subjects Protections Policy Institutional Review Board Statement of Ethical Principles Missouri Southern State University is committed to quality teaching and learning, scholarshi Add to Reading List Source URL: www.mssu.edu Language: English - Date: 2012-10-18 13:55:05 Health Institutional review board Investigational Device Exemption Clinical trial Investigational New Drug Declaration of Helsinki National Institutes of Health Human subject research Public Responsibility in Medicine and Research Clinical research Research Medicine
766	October 25, [removed]submitted electronically at www.regulations.gov) Jerry Menikoff, MD, JD Office for Human Research Protections Add to Reading List Source URL: www.acponline.org Language: English - Date: 2013-03-01 09:43:11 Applied ethics Medical ethics Design of experiments Pharmacology Drug safety Institutional review board Human subject research Informed consent Office for Human Research Protections Clinical research Ethics Research
767	- A Primer for Members of Community AdvisoRy committees in HIV Clinical Trials & observational studies Add to Reading List Source URL: www.hivnet.ubc.ca Language: English - Date: 2010-12-15 18:44:01 Applied ethics Research ethics Medical ethics Design of experiments Pharmacology Clinical trial Informed consent Clinical research ethics Human subject research Clinical research Research Ethics
768	“The encouragement, support and adult stutterers’ testimonies were priceless.” – a Parent “I wish my child could feel like he does today… Add to Reading List Source URL: www.westutter.org Language: English - Date: 2014-09-03 12:50:26 National Stuttering Association Medicine Psychiatry Human subject research in the United States Cultural references to stuttering Stuttering therapy Dyslexia Stuttering Human communication
769	SAMPLE CONSENT FORMS TEMPLATE E: FACULTY/STAFF INVESTIGATOR - INFORMED CONSENT NOTICE AND ADULT SUBJECTS University of North Texas Institutional Review Board Informed Consent Notice Add to Reading List Source URL: research.unt.edu Language: English - Date: 2014-08-22 16:23:25 Research Applied ethics Research ethics Design of experiments Pharmacology Institutional review board Informed consent Human subject research Clinical research coordinator Clinical research Medical ethics Ethics
770	RTF Document Add to Reading List Source URL: www.iue.edu Language: English - Date: 2010-04-28 08:42:48 Research Science Design of experiments Pharmacology Pharmaceutical industry Institutional review board Informed consent Human subject research Psychology Clinical research Ethics Medical ethics

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