IRB: Ethics - PDFSEARCH.IO - Document Search Engine

IRB: Ethics
Results: 397

#	Item
211	IRB Project Closure Form Instructions: Complete this form when an approved human participant research project is CONCLUDED or CANCELLED. Projects that involve long-term follow-up of participants must remain open, even if Add to Reading List Source URL: www.irb.cornell.edu Language: English - Date: 2013-09-18 12:22:43 Drug safety Institutional review board Ethics Scientific method Science Clinical research Design of experiments Pharmacology
212	COLUMBIA UNIVERSITY MEDICAL CENTER INSTITUTIONAL REVIEW BOARD (IRB) PROCEDURES TO COMPLY WITH PRIVACY LAWS THAT AFFECT USE AND DISCLOSURE OF PROTECTED HEALTH INFORMATION FOR RESEARCH PURPOSES Procedures Add to Reading List Source URL: www.cumc.columbia.edu Language: English - Date: 2013-01-08 12:22:13 Privacy law Health Science Design of experiments Pharmacology Institutional review board Health Insurance Portability and Accountability Act Information privacy Internet privacy Ethics Clinical research Data privacy
213	IRB Children supp. Version 2 Add to Reading List Source URL: archive.hhs.gov Language: English - Date: 2005-08-30 07:32:18 Medical ethics Design of experiments Pharmacology Research ethics Institutional review board Human subject research Consent Precocious puberty Ethical problems using children in clinical trials Ethics Clinical research Research
214	-[removed]Institutional Review Board for the Protection of Human Subjects (IRB) REQUEST FOR CONTINUING REVIEW Add to Reading List Source URL: www.wesley.edu Language: English - Date: 2013-07-25 09:44:47 Institutional review board Pharmacology Click consonant Ethics Approval voting Science Applied ethics Clinical research Design of experiments Drug safety
215	UNIVERSITY OF NORTH DAKOTA -- INSTITUTIONAL REVIEW BOARD -- STANDARD OPERATING PROCEDURES COMPOSITION OF THE IRB SOP #: 201 Add to Reading List Source URL: und.edu Language: English - Date: 2014-06-24 16:40:24 Drug safety Institutional review board Ethics Scientific method Research Public Responsibility in Medicine and Research Clinical research Design of experiments Pharmacology
216	UNIVERSITY OF NORTH DAKOTA -- INSTITUTIONAL REVIEW BOARD -- STANDARD OPERATING PROCEDURES MANAGEMENT OF IRB PERSONNEL SOP #: 105 Add to Reading List Source URL: und.edu Language: English - Date: 2011-01-26 11:37:59 Drug safety Institutional review board Ethics Scientific method Research Instituto de Resseguros do Brasil Clinical research Design of experiments Pharmacology
217	Comparison of Existing Rules with Some of the Changes Being Considered Current rule Issue 1: There are no specific data security protections for IRB-reviewed research: regulations require IRBs to determine, for each stud Add to Reading List Source URL: und.edu Language: English - Date: 2011-09-09 15:11:07 Science Institutional review board Human subject research Cooperative Human Tissue Network Clinical research Research Ethics
218	UNIVERSITY OF NORTH DAKOTA -- INSTITUTIONAL REVIEW BOARD -- STANDARD OPERATING PROCEDURES MANAGEMENT OF THE IRB SOP #: 202 Add to Reading List Source URL: und.edu Language: English - Date: 2011-01-26 11:40:39 Drug safety Institutional review board Ethics Scientific method Research Instituto de Resseguros do Brasil International Rugby Board Clinical research Design of experiments Pharmacology
219	SCDMH INSTITUTIONAL REVIEW BOARD CONTINUING REVIEW OF RESEARCH PROJECT ORA Use Only IRB PROJECT NO.: Add to Reading List Source URL: www.state.sc.us Language: English - Date: 2013-12-06 14:27:21 Applied ethics Medicine Drug safety Design of experiments Pharmacology Institutional review board Informed consent Clinical research coordinator Ethical research in social science Clinical research Medical ethics Research
220	Microsoft PowerPoint - Joan ShapiroTHE IRB PROCESS Workshop[removed]ppt Add to Reading List Source URL: www.azdhs.gov Language: English - Date: 2011-08-05 15:03:33 Science Design of experiments Pharmacology Medical ethics Pharmaceutical industry Institutional review board Clinical trial Informed consent Human subject research Clinical research Research Ethics

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