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Research ethics
Results: 14789

#	Item
571	Instructions: These DoD and DON 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 checkli Add to Reading List Source URL: humansubjects.stanford.edu Language: English - Date: 2013-09-20 10:28:01 Medical research Medical ethics Clinical research ethics Applied ethics Research Human subject research Clinical research Research ethics Public Responsibility in Medicine and Research Informed consent Experimentation on prisoners Consent
572	Instructions: These EPA 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 eP Add to Reading List Source URL: humansubjects.stanford.edu Language: English - Date: 2013-05-29 11:32:55 Medical ethics Applied ethics Clinical research Human subject research Research United States Environmental Protection Agency Common Rule
573	—•— Institutional Ethics Requirements and Anthropological Research Techniques, or, why I want to join a university ethics committee Add to Reading List Source URL: explusultra.wun.ac.uk Language: English - Date: 2009-11-29 18:11:48
574	Family y St e l Engineering Add to Reading List Source URL: static.nsta.org Language: English - Date: 2013-05-31 14:41:05 Engineering Ethics Philosophy of science Education Engineering education Science and technology Engineering education research Schulich School of Engineering
575	Stanford University HRPP Informed Consent Checklist Medical Research, Clinical Investigations CHK-C1m 1/4 Add to Reading List Source URL: humansubjects.stanford.edu Language: English - Date: 2014-06-26 16:17:02 Medical research Clinical research Clinical research ethics Pharmaceutical industry Medical ethics Design of experiments Clinical trial Title 1 of the Code of Federal Regulations Health Insurance Portability and Accountability Act Informed consent
576	Informed consent information should be consistent with procedures, etc. as described in eProtocol application VA research: Refer to CHK-7 VA Research and AID-27m Reviewing VA Research for additional requirements Regul Add to Reading List Source URL: humansubjects.stanford.edu Language: English - Date: 2014-08-06 19:30:22 Medical research Clinical research Clinical research ethics Pharmaceutical industry Medical ethics Design of experiments Title 1 of the Code of Federal Regulations Clinical trial Health Insurance Portability and Accountability Act Informed consent
577	Spring 2012 Events MARCH 6: RESEARCH ETHICS GRAND ROUNDS – “Moral Frameworks for Animal Research.” Rebecca Walker, PhD, Associate Professor, Department of Social Medicine, University of North Carolina School of Med Add to Reading List Source URL: bioethics.wfu.edu Language: English - Date: 2012-03-02 09:29:46
578	THE UNIVERSITY OF HONG KONG Human Research Ethics Committee Add to Reading List Source URL: www.rss.hku.hk Language: English - Date: 2016-01-04 23:10:32 Medical ethics Clinical research ethics Human subject research Autonomy Clinical research Informed consent Institutional review board Consent Medical privacy Research Internet Psychology
579	Peer Review Ethics and Politics; or, how to review something you hate. Jonathan Sterne Microsoft Research / McGill University http://st Add to Reading List Source URL: sterneworks.org Language: English - Date: 2014-01-21 14:57:02
580	Protocol Director: Protocol: Name of Test Article: include IND/IDE Number, if applicable Add to Reading List Source URL: humansubjects.stanford.edu Language: English - Date: 2012-02-06 15:25:51 Medical ethics Medical research Clinical research ethics Applied ethics Ethics Human subject research Informed consent Consent

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