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Human subject research
Results: 1674

#	Item
211	Microsoft Word - Code of Ethics Add to Reading List Source URL: www.embs.org Language: English - Date: 2015-12-11 09:17:55 Clinical research Medical ethics Research ethics Good laboratory practice Organisation for Economic Co-operation and Development Human subject research Pharmaceutical industry
212	VCC Choice and Consent Working Group, draft: May 31, 2013 _____________________________________________________________________________________________ CHOICE AND CONSENT – Requirements related to the customer’s gran Add to Reading List Source URL: www.smartgrid.gov Language: English - Date: 2015-02-12 06:56:48 Medical ethics Autonomy Identity management Human subject research Informed consent Consent Internet privacy Privacy
213	Instructions: These DOJ requirements differ from or are additional to our current HRPP policies and must be met prior to initiating human research activities, when applicable. IRB Manager: Attach this checklist in ePr Add to Reading List Source URL: humansubjects.stanford.edu Language: English - Date: 2013-05-29 11:32:05 Medical ethics Medical research Applied ethics Autonomy Research Clinical research ethics Clinical research Human subject research Consent Informed consent
214	An organization’s employees or agents refers to individuals who: (1) act on behalf of the institution; (2) exercise institutional authority or responsibility; or (3) perform institutionally designated activities. “E Add to Reading List Source URL: humansubjects.stanford.edu Language: English - Date: 2013-05-07 11:04:12 Medical research Research Health Clinical research Medical ethics Research ethics Design of experiments Clinical trial Human subject research Food and Drug Administration Informed consent
215	DOCUMENTATION OF TRAINING IN HUMAN SUBJECT PROTECTION (FOR INVESTIGATORS AND DIRECTORS) Institutional Review Board The Federal Office for Human Research Protections (OHRP) requires Principle Investigators of Add to Reading List Source URL: www.virginiawestern.edu Language: English - Date: 2015-04-01 12:10:55
216	THE APPROVAL PROCESS 1. If the proposal is determined a human subject research project, the PI completes the IRB review application. 2. The PI gathers all required documentation as per the application checklist. 3. The P Add to Reading List Source URL: www.virginiawestern.edu Language: English - Date: 2014-11-10 16:29:16
217	Wayne State University Institutional Review Board Subject Department of Defense Requirements for Human Subject Research Protection (Policy 06-06) Add to Reading List Source URL: irb.wayne.edu Language: English - Date: 2015-04-29 11:45:42
218	APPENDIX 2 INFORMATION SOURCES Add to Reading List Source URL: www.defense.gov Language: English - Date: 2007-03-30 18:17:25 Health Advisory Committee on Human Radiation Experiments Human radiation experiments Nuclear physics United States Department of Defense Ionizing radiation United States Department of Energy Human subject research in the United States Radiobiology Medicine
219	CUNY UI IRB and the Baruch HRPP Add to Reading List Source URL: www.baruch.cuny.edu Language: English - Date: 2015-02-25 16:51:08 Applied ethics Medical ethics Design of experiments Pharmacology Research ethics Institutional review board Belmont Report Human subject research City University of New York Clinical research Ethics Research
220	ETHICAL GUIDELINES FOR EPIDEMIOLOGICAL RESEARCH Add to Reading List Source URL: www.niph.go.jp Language: English - Date: 2010-07-20 01:41:58 Research ethics Ethics Medical ethics Epidemiology Medical research Declaration of Helsinki Informed consent Human subject research Clinical trial Clinical research Research Health

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