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Human subject research
Results: 1674

#	Item
151	Microsoft Word - SOP - Exempt Process Case Reports.doc Add to Reading List Source URL: research.missouri.edu Language: English - Date: 2015-07-01 12:43:02 Clinical research ethics Medical ethics Design of experiments Clinical research Institutional review board Human subject research Food and Drug Administration Grant Health Insurance Portability and Accountability Act Office for Human Research Protections Clinical research coordinator
152	Addendum 2 DEPARTMENTAL ETHICS SCREENING COMMITTEE (DESC) CHECKLIST Add to Reading List Source URL: www.ekon.sun.ac.za Language: English - Date: 2012-06-04 10:01:36 Medical ethics Clinical research ethics Human subject research Professional ethics Institutional review board Research ethics Ethics Informed consent Public Responsibility in Medicine and Research Research Artificial intelligence
153	Regulations for use of Clinical Research databases, data and biomaterial samples Regulations for use of Clinical Research databases, data and biomaterial samples of the DZNE By resolution of the Clinical Board of 20 July Add to Reading List Source URL: www.dzne.de Language: English - Date: 2016-06-13 10:04:50 Clinical research Pharmaceutical industry Design of experiments Human subject research Medical ethics German Center for Neurodegenerative Diseases Clinical trial Institutional review board Good clinical practice Informed consent
154	subject_pools_chapter_7.dvi Add to Reading List Source URL: cess.nyu.edu Language: English - Date: 2009-10-13 18:45:18 Validity Causal inference Experiments Game theory Design of experiments Experimental economics External validity Internal validity Construct validity Experiment Human subject research Ecological validity
155	Institutional Review Board Guidebook * CHAPTER I * INSTITUTIONAL ADMINISTRATION A. Jurisdiction of the Institutional Review Board Add to Reading List Source URL: ccnmtl.columbia.edu Language: English - Date: 2007-10-05 14:09:59 Clinical research Design of experiments Medical ethics Research ethics Institutional review board Public Responsibility in Medicine and Research Clinical research coordinator Clinical trial Declaration of Helsinki Human subject research Ethics committee Grant
156	Report of the Working Party on Conducting Research on the internet Add to Reading List Source URL: www.psy.ed.ac.uk Language: English - Date: 2011-06-10 11:47:55 Human subject research Medical ethics Clinical research ethics Research ethics Experimental psychology Informed consent Debriefing Research participant Online interview Deception Interview Qualitative research
157	January 10, 2001 Draft Interim Guidance FINANCIAL RELATIONSHIPS IN CLINICAL RESEARCH: ISSUES FOR INSTITUTIONS, CLINICAL INVESTIGATORS, AND IRBs TO CONSIDER WHEN DEALING WITH ISSUES OF Add to Reading List Source URL: ccnmtl.columbia.edu Language: English - Date: 2007-10-05 14:09:59 Clinical research ethics Clinical research Medical ethics Design of experiments Human subject research Clinical trial Institutional review board Office for Human Research Protections Informed consent Conflict of interest Public Responsibility in Medicine and Research
158	Microsoft Word - FERCAP Newsletter - February 2010.doc Add to Reading List Source URL: www.fercap-sidcer.org Language: English - Date: 2010-03-07 04:38:53 Medical ethics Clinical research ethics Design of experiments Clinical research Human subject research Institutional review board Ethics committee Clinical trial Scientific misconduct Informed consent Public Responsibility in Medicine and Research Outline of ethics
159	Intel International Science and Engineering Fair International Rules and Guidelines 2017 Add to Reading List Source URL: www.sefi.org Language: English - Date: 2016-06-23 02:19:02 Medical ethics Clinical research ethics Human subject research Intel International Science and Engineering Fair Society for Science and the Public Research ethics Institutional review board Science fair Intel Informed consent Meanings of minor planet names: 2100122000 Meanings of minor planet names: 2300124000
160	Microsoft Word - SOP - Post Approval Monitoring Process.doc Add to Reading List Source URL: research.missouri.edu Language: English - Date: 2015-07-01 12:50:34 Medical ethics Clinical research ethics Human subject research Clinical research Design of experiments Institutional review board Informed consent Clinical research coordinator Public Responsibility in Medicine and Research

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