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Office for Human Research Protections
Results: 393

#	Item
11	U seful Links for U H Investigators Human Studies Program Website Add to Reading List Source URL: www.fmp.hawaii.edu Language: English - Date: 2014-07-29 17:16:13 Clinical research ethics Clinical research Pharmaceutical industry Design of experiments Office for Human Research Protections ClinicalTrials.gov Clinical trial
12	Microsoft Word - Unanticipated_Problems Add to Reading List Source URL: www.firstclinical.com Language: English - Date: 2014-09-14 03:12:34 Clinical research Pharmaceutical industry Design of experiments Medical ethics Institutional review board Clinical trial Pharmacovigilance Office for Human Research Protections Adverse event Human subject research Serious adverse event Adverse effect
13	Research discoveries can improve people’s health. For more information call: Before you decide to become a research Add to Reading List Source URL: publicfiles.jaeb.org Language: English - Date: 2014-02-10 13:44:14 Clinical research ethics Medical ethics Clinical research Research ethics Office for Human Research Protections Human subject research United States Department of Health and Human Services Research Clinical research coordinator Cooperative Human Tissue Network
14	Compensation for Research Participation HRPP GUIDELINE 203 Issuing Office: Office of Research Administration Responsible Officer: Human Protections Administrator Add to Reading List Source URL: www.irb.purdue.edu Language: English - Date: 2014-06-04 09:41:11 Clinical research ethics Public Responsibility in Medicine and Research Federal Insurance Contributions Act tax Clinical research Institutional review board
15	The IRB staff and the IRBs have the following written policies and procedures for determining the risks to vulnerable populations as defined in applicable federal regulations, and specifically for determining the require Add to Reading List Source URL: researchcompliance.stanford.edu Language: English - Date: 2016-04-12 01:21:50 Clinical research ethics Contact Office for Human Research Protections
16	Volume 11, Number 5 • MayNews and Analysis for Colleges, Universities and Teaching Hospitals Contents a COI: The Add to Reading List Source URL: eelegal.org Language: English - Date: 2016-02-11 15:56:55 Medical ethics Clinical research ethics Human subject research Clinical research Office for Human Research Protections Research ethics Institutional review board Tuskegee syphilis experiment United States Office of Research Integrity Justice National Institutes of Health The Humane Society of the United States
17	§ CFR Ch. I (4–1–12 Edition) (3) Requesting that the applicant conduct additional independent studies Add to Reading List Source URL: publicfiles.jaeb.org Language: English - Date: 2014-01-30 11:37:27 Clinical research Pharmaceutical industry Food and Drug Administration Design of experiments Institutional review board Clinical trial Public Responsibility in Medicine and Research Investigational device exemption Office for Human Research Protections Clinical investigator Human subject research Covered clinical study
18	Microsoft Word - SOP - Reporting Requirements.doc Add to Reading List Source URL: research.missouri.edu Language: English Clinical research ethics Institutional review board Office for Human Research Protections Grant IRB Protocol Common Rule Clinical research coordinator Public Responsibility in Medicine and Research
19	Microsoft Word - SOP - Exempt Process Case Reports.doc Add to Reading List Source URL: research.missouri.edu Language: English - Date: 2015-07-01 12:43:02 Clinical research ethics Medical ethics Design of experiments Clinical research Institutional review board Human subject research Food and Drug Administration Grant Health Insurance Portability and Accountability Act Office for Human Research Protections Clinical research coordinator
20	January 10, 2001 Draft Interim Guidance FINANCIAL RELATIONSHIPS IN CLINICAL RESEARCH: ISSUES FOR INSTITUTIONS, CLINICAL INVESTIGATORS, AND IRBs TO CONSIDER WHEN DEALING WITH ISSUES OF Add to Reading List Source URL: ccnmtl.columbia.edu Language: English - Date: 2007-10-05 14:09:59 Clinical research ethics Clinical research Medical ethics Design of experiments Human subject research Clinical trial Institutional review board Office for Human Research Protections Informed consent Conflict of interest Public Responsibility in Medicine and Research