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IRB: Ethics
Results: 397

#	Item
241	IRB Appendix Model Volunteer Consent Documents for the Indian Health Service - 2nd Ed William L. Freeman, MD, MPH Chair, National IHS IRB OCT 1, 2000 Explanation Add to Reading List Source URL: www.npaihb.org Language: English - Date: 2006-06-15 22:18:00 Research Design of experiments Pharmacology Medical ethics Clinical trial Pharmaceutical industry Informed consent Vaccine Clinical research Medicine Health
242	Version Date[removed]Faculty Senate Approved INSTITUTIONAL REVIEW BOARD FWA: [removed] \| IRB: [removed] Add to Reading List Source URL: www.pacificu.edu Language: English - Date: 2014-11-26 19:43:48 Applied ethics Institutional review board Investigational New Drug Investigational Device Exemption Public Responsibility in Medicine and Research Declaration of Helsinki Belmont Report Adverse event Clinical research coordinator Clinical research Research Medicine
243	IRB Children supp. Version 2 Add to Reading List Source URL: www.fda.gov Language: English - Date: 2005-10-11 13:44:31 Medical ethics Design of experiments Pharmacology Research ethics Institutional review board Human subject research Consent Ethical problems using children in clinical trials Informed consent Ethics Clinical research Research
244	Interpretation of the Convention Refugee Definition in the Case Law - Chapter 10 - Addendum #1 Add to Reading List Source URL: www.irb-cisr.gc.ca Language: English - Date: 2013-09-28 10:42:55 Criminal law War crime Crimes against humanity International criminal law Ethics International law
245	-[removed] Institutional Review Board for the Protection of Human Subjects Purpose The Institutional Review Board (IRB) for the Protection of Human Subjects is the regulatory body of Wesley Co Add to Reading List Source URL: www.wesley.edu Language: English - Date: 2013-07-17 13:29:56 Ethics Medical ethics Institutional review board Belmont Report Public Responsibility in Medicine and Research Human subject research Office for Human Research Protections Informed consent National Commission for the Protection of Human Subjects of Biomedical and Behavioral Research Clinical research Research Medicine
246	Commonwealth of Massachusetts Department of Mental Health Unaffiliated Research Investigator Agreement Name of Institution Providing IRB Oversight: Department of Mental Health OHRP Federal wide Assurance Number: FWA00000 Add to Reading List Source URL: www.mass.gov Language: English - Date: 2014-07-31 12:15:26 Applied ethics Belmont Report Human subject research Office for Human Research Protections Food and Drug Administration Institutional review board Clinical research coordinator Clinical research Research Ethics
247	Microsoft Word - IRB research consent_5.doc Add to Reading List Source URL: dnatesting.uchicago.edu Language: English - Date: 2014-01-28 12:05:07 Science Applied ethics Design of experiments Pharmacology Genetic testing Institutional review board Misattributed paternity Clinical trial Medical ethics Clinical research Medicine
248	Table: Study IRB and consent features across WMH Survey Initiative Type of Organization IRB/Ethics approval Type of Add to Reading List Source URL: www.hcp.med.harvard.edu Language: English - Date: 2013-04-24 16:35:56 Design of experiments Pharmacology Scientific method Drug safety Institutional review board Medical ethics Medical school Ethics Committee Clinical research Ethics Research
249	Guidance for Industry IRB Review of Stand-Alone HIPAA Authorizations Under FDA Regulations FINAL GUIDANCE This guidance is being distributed for immediate implementation. Add to Reading List Source URL: www.fda.gov Language: English - Date: 2003-11-05 16:47:36 Research Clinical research Data privacy Health Insurance Portability and Accountability Act Privacy law Medical statistics Food and Drug Administration Privacy Institutional review board Health Ethics Pharmacology
250	Data Request Approval Process All requestors are to submit the Confidential Data Request Application. Incomplete or insufficient applications will be rejected. The Research Collaborative Internal Review Board (IRB) revie Add to Reading List Source URL: www.mi.gov Language: English - Date: 2013-08-01 11:58:40 Research Scientific method Drug safety Institutional review board Ethics Clinical research Design of experiments Pharmacology

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