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Human subject research
Results: 1674

#	Item
191	Minimum Criteria for ICH E6 GCP Investigator Site Personnel Training (Excerpt from TransCelerate BioPharma Operating Principles) Scope The intent of this document is to define the Minimum Criteria for Good Clinical Pract Add to Reading List Source URL: www.transceleratebiopharmainc.com Language: English - Date: 2015-12-07 16:54:46 Medical research Clinical research Pharmaceutical industry Good clinical practice Adverse event Source document Public Responsibility in Medicine and Research Informed consent Inclusion and exclusion criteria Serious adverse event Human subject research Trial master file
192	VIRGINIA DEPARTMENT OF CORRECTIONS Human Subject Research and Review Committee EXTERNAL RESEARCH PROJECTS Research Proposal Note: This is a sample outline to use as a guide in completing your Research Proposal. Add to Reading List Source URL: vadoc.virginia.gov Language: English - Date: 2013-07-30 14:44:04
193	VCC Choice and Consent Working Group, draft: 6-Sep-13 _____________________________________________________________________________________________ CHOICE AND CONSENT – Policy principles related to the customer’ Add to Reading List Source URL: www.smartgrid.gov Language: English - Date: 2015-02-12 06:56:56 Medical ethics Autonomy Ethics Identity management Applied ethics Law Human subject research Informed consent Privacy Internet privacy Consent
194	amended THE UNIVERSITY OF HONG KONG Human Research Ethics Committee Operational Guidelines and Procedures I. Add to Reading List Source URL: www.rss.hku.hk Language: English - Date: 2016-01-07 02:10:38 Medical ethics Clinical research ethics Clinical research Human subject research Design of experiments Informed consent Institutional review board Research ethics Clinical trial Ethics committee Consent Psychology
195	Stanford University HRPP Exemption Eligibility Determining if Human Subject Research is Exempt from Regulations CHKProtocol Director: Protocol ID: Add to Reading List Source URL: humansubjects.stanford.edu Language: English - Date: 2013-06-24 15:05:58 Identity management Law Privacy Medical privacy
196	ORahs Users Manual For Investigators The Office of Research Human Subjects staff have created this manual to assist investigators with ORahs e-submission of research for review and approval by the UCSB Human Subjects Com Add to Reading List Source URL: www.research.ucsb.edu Language: English - Date: 2014-11-18 12:38:46 Research Knowledge Clinical research ethics Clinical research Science Medical ethics Human subject research Research Development Electronic submission Common Rule Institutional review board
197	Protocol ID: Protocol Director: Met Not Met waived Add to Reading List Source URL: humansubjects.stanford.edu Language: English - Date: 2012-12-17 13:22:44 Medical research Medical ethics Autonomy Clinical research ethics Law Ethics Human subject research Consent Tort law Informed consent Health Insurance Portability and Accountability Act
198	ADVANCE FOR RESEARCH SUBJECT PAYMENTS This form is to be used only for the request of cash payments made to human subjects participating in research projects that have been reviewed and approved by FIU’s Institutional Add to Reading List Source URL: research.fiu.edu Language: English - Date: 2016-01-25 17:04:32
199	Protocol ID: PD: Meeting Date: Remember! Check IRB Administrative Notes in eProtocol Checklist completed by (IRB Staff name): Add to Reading List Source URL: humansubjects.stanford.edu Language: English - Date: 2016-02-25 19:35:04 Clinical research ethics Human subject research Medical ethics Informed consent Yes Research Music Performing arts
200	Workshop on Wearable Human Biomechanical Analysis for Healthcare Applications The study of human biomechanics has been a subject of significant research interest, as we seek to understand and improve the performance of t Add to Reading List Source URL: www.bsn2015.org Language: English - Date: 2015-04-22 20:24:00

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