IRB: Ethics - PDFSEARCH.IO - Document Search Engine

IRB: Ethics
Results: 397

#	Item
251	Oral History, IRB and Information Risk: A Response to the Federal Proposal As some of you may know, the federal government has requested comment on proposed changes to the Common Rule, which regulates research on what ar Add to Reading List Source URL: www.oralhistory.org Language: English - Date: 2011-12-13 15:03:54 Science Drug safety Institutional review board Ethics Scientific method Oral history Oral History Association Clinical research Design of experiments Pharmacology
252	IRB Preliminary Approval or Waiver for Graduate Thesis Before you start your research All research involving living human beings or bodily tissue samples requires advance approval from AUC’s Institutional Review Board Add to Reading List Source URL: www.aucegypt.edu Language: English - Date: 2014-07-01 09:11:39 Ethics Design of experiments Drug safety Institutional review board Pharmacology Thesis Doctor of Philosophy Graduate school Knowledge Education Clinical research
253	RESEARCH SUBJECTS INFORMATION UPDATED CUMC INSTITUTIONAL REVIEW BOARD (IRB) CONTACT INFORMATION The Columbia University Medical Center (CUMC) Institutional Review Board (IRB) is a committee that independently conducts on Add to Reading List Source URL: cumc.columbia.edu Language: English - Date: 2013-10-16 13:31:46 Medical ethics Applied ethics Design of experiments Pharmacology Drug safety Institutional review board Informed consent Human subject research Clinical research coordinator Clinical research Research Ethics
254	Proof of IRB Approval or Waiver for Completed Graduate Thesis To be submitted with completed thesis and other forms requested below All research involving living human beings or bodily tissue samples requires advance app Add to Reading List Source URL: www.aucegypt.edu Language: English - Date: 2014-07-01 09:11:39 Rhetoric Thesis Ethics Clinical research Institutional review board Knowledge Education Academia
255	DOC Document Add to Reading List Source URL: www.trinitydc.edu Language: English - Date: 2013-09-18 21:04:31 Science Institutional review board Office for Human Research Protections Human subject research Cooperative Human Tissue Network Certified IRB Professional Clinical research Research Ethics
256	Request for Waivers of Informed Consent (To be submitted with Application for IRB Review of Research) Under special circumstances, investigators can request one of two kinds of waivers to obtaining written informed conse Add to Reading List Source URL: www.nd.gov Language: English - Date: 2008-02-22 15:17:44 Applied ethics Research Informed consent Autonomy Research ethics Consent Human subject research Institutional review board Ethics Clinical research Medical ethics
257	SPS IRB Frequently Asked Questions What is an IRB? The Institutional Review Board is a committee to oversee the ethical principles underlying the conduct of biomedical and behavioral research with human subjects. Trini Add to Reading List Source URL: www.trinitydc.edu Language: English - Date: 2013-09-18 21:04:13 Applied ethics Design of experiments Pharmacology Drug safety Institutional review board National Institutes of Health Deception Human subject research Research ethics Clinical research Ethics Research
258	Request for Waivers of Informed Consent (To be submitted with Application for IRB Review of Research) Under special circumstances, investigators can request one of two kinds of waivers to obtaining written informed conse Add to Reading List Source URL: www.nd.gov Language: English - Date: 2008-02-22 15:17:59 Applied ethics Research Informed consent Autonomy Research ethics Consent Human subject research Institutional review board Ethics Clinical research Medical ethics
259	HUMAN RESEARCH PROTECTION PROGRAM Add to Reading List Source URL: www.irb.cornell.edu Language: English - Date: 2013-09-18 12:22:55 Applied ethics Institutional review board Public Responsibility in Medicine and Research Declaration of Helsinki Human subject research Belmont Report Office for Human Research Protections Cornell University Research Development Clinical research Research Ethics
260	Columbia University IRB New page: Informed Consent (required for all studies) Select all that apply: Add to Reading List Source URL: www.columbia.edu Language: English - Date: 2013-08-20 10:24:07 Medical ethics Behavior Informed consent Consent Research Ethics Autonomy Clinical research

UPDATE