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Human subject research
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91	This story was printed from DailyPennsylvanian.com. Site URL: http://www.dailypennsylvanian.com. Researcher Wilson to step down as IHGT head The Institute for Human Gene Therapy came under fire after the death of an 18-y Add to Reading List Source URL: ccnmtl.columbia.edu Language: English - Date: 2007-10-05 14:09:59 Biology Biotechnology Human subject research in the United States Jesse Gelsinger Gene delivery Medical research Gelsinger Gene therapy Virology Therapy James Wilson Stem cell
92	FAHSS Research Ethics Committee Application form Name of Lead Researcher: _________________________ April 2015 FAHSS Research Ethics Committee Add to Reading List Source URL: ahss.tcd.ie Language: English - Date: 2015-05-06 11:09:25 Applied ethics Clinical research ethics Ethics Medical research Medical ethics Human subject research Professional ethics Design of experiments Informed consent Institutional review board Research ethics Research
93	APPLICATION TO THE UNIVERSITY OF MISSOURI-ROLLA CAMPUS INSTITUTIONAL REVIEW BOARD FOR THE PROTECTION OF HUMAN SUBJECTS IN RESEARCH (UMRIRB-1) Review Requested: Exemption Add to Reading List Source URL: irb.mst.edu Language: English - Date: 2014-01-22 05:22:59 Medical research Medical ethics Applied ethics Clinical research ethics Ethics Human subject research Clinical research Design of experiments Institutional review board Public Responsibility in Medicine and Research Informed consent Psychology
94	H3Africa Guidelines for Informed Consent Developed by the H3Africa Working Group on Ethics and Regulatory Issues for the Human Heredity and Health in Africa (H3Africa) Consortium Second Edition September 2014 Add to Reading List Source URL: h3africa.org Language: English - Date: 2014-10-24 11:44:51 Applied ethics Medical ethics Ethics Medical research Human subject research Clinical research ethics Research ethics Design of experiments Public Responsibility in Medicine and Research Informed consent Biobank Institutional review board
95	Human Participants Form (4) Required for all research involving human participants not at a Regulated Research Institution. If at a Regulated Research Institution, use institutional approval forms for documentation of p Add to Reading List Source URL: www.ncsciencefair.org Language: English - Date: 2016-01-20 11:06:54 Clinical research ethics Medical research Medical ethics Human subject research Ethics Applied ethics Design of experiments Institutional review board Informed consent
96	Purdue HRPP – Guidance and Procedure Recruitment of Human Participants Version Effective Date Add to Reading List Source URL: www.irb.purdue.edu Language: English - Date: 2014-07-24 10:43:34 Medical ethics Human subject research Clinical research Design of experiments Clinical trial Institutional review board Public Responsibility in Medicine and Research Recruitment Snowball sampling Research participant Informed consent Patient recruitment
97	Stanford University What Qualifies as Human Subject Research HRPP Policy Guidance Add to Reading List Source URL: researchcompliance.stanford.edu Language: English - Date: 2016-04-12 01:21:49 Clinical research Pharmaceutical industry Design of experiments Medical ethics Research ethics Clinical trial Human subject research Food and Drug Administration Research Institutional review board Clinical research coordinator
98	Package ‘sdcMicro’ July 18, 2014 Type Package Title Statistical Disclosure Control methods for anonymization of microdata and risk estimation VersionDate Add to Reading List Source URL: www.ihsn.org Language: English - Date: 2014-10-08 15:37:02 Disclosure Human subject research Statistical disclosure control Microdata Risk
99	REVISED ETHICAL GUIDELINES FOR EDUCATIONAL RESEARCH (2004) REVISED ETHICAL GUIDELINES FOR EDUCATIONAL RESEARCH (2004) Add to Reading List Source URL: www.edrsr.co.nz Language: English - Date: 2013-01-21 19:11:02 Clinical research ethics Medical ethics Human subject research Research ethics Design of experiments Public Responsibility in Medicine and Research Informed consent Institutional review board Research Ethical research in social science
100	IRB Compliance With Regulation FERCAP International Conference Dr. Brad Waite Coordinator, International IRB Fellowship Western Institutional Review Board (WIRB) Add to Reading List Source URL: www.fercap-sidcer.org Language: English - Date: 2010-02-19 02:38:03 Medical ethics Clinical research Research ethics Applied ethics Institutional review board Council for International Organizations of Medical Sciences Evaluation Human subject research Food and Drug Administration

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