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Clinical research coordinator
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#	Item
361	For IRB use only #: Sub date: Submit Add to Reading List Source URL: www2.humboldt.edu Language: English - Date: 2012-10-18 14:54:03 Pharmaceutical industry Research Pharmacology Scientific method Science Clinical research coordinator Institutional review board Clinical research Grants Philanthropy
362	Florida Gulf Coast University Institutional Review Board Office of Research and Graduate Studies Howard Hall, suite[removed]7522 Add to Reading List Source URL: www.fgcu.edu Language: English - Date: 2013-12-18 11:04:36 Design of experiments Pharmacology Health Pharmaceutical industry Medical ethics Institutional review board Clinical trial Clinical research coordinator Ethical research in social science Clinical research Research Science
363	Investigator Guidelines for Research that Includes Human Subjects I. Where Do I Begin? UMF faculty, staff, and students who intend to conduct projects involving human participants must seek prospective approval (or an e Add to Reading List Source URL: www2.umf.maine.edu Language: English - Date: 2014-06-05 15:57:10 Pharmacology Drug safety Scientific method Science Institutional review board Clinical research coordinator Guidelines for human subject research Clinical research Research Design of experiments
364	42 USC 282 NB: This unofficial compilation of the U.S. Code is current as of Jan. 4, 2012 (see http://www.law.cornell.edu/uscode/uscprint.html). TITLE 42 - THE PUBLIC HEALTH AND WELFARE CHAPTER 6A - PUBLIC HEALTH SERVICE Add to Reading List Source URL: www.law.cornell.edu Language: English - Date: 2013-07-17 17:59:32 Pharmaceutical industry Medicine Nursing research National Institutes of Health Design of experiments Clinical trial Medical research ClinicalTrials.gov Clinical research coordinator Research Health Clinical research
365	INSTITUTIONAL REVIEW BOARD Exemption application for research with human participants This form is to be completed if you are conducting a research project involving human participants, and you think the project is exemp Add to Reading List Source URL: www.providence.edu Language: English - Date: 2015-01-12 23:35:27 Medical ethics Applied ethics Design of experiments Pharmacology Drug safety Institutional review board Informed consent Human subject research Clinical research coordinator Clinical research Research Ethics
366	Is it Human Subjects Research? Institutional Review Board (IRB) Policy Statement University of Maine at Farmington August 27, 2008 In accordance with University of Maine System policies and Federal regulations, all rese Add to Reading List Source URL: www2.umf.maine.edu Language: English - Date: 2014-06-05 15:57:10 Applied ethics Institutional review board Human subject research Guidelines for human subject research Clinical research coordinator Clinical research Research Ethics
367	SUNY Upstate Medical University Research Administration Quality Assessment & Improvement Program (QAIP) Compliance Tips Common Mistakes: Regulatory documentation: Add to Reading List Source URL: www.upstate.edu Language: English - Date: 2011-03-31 11:16:56 Informed consent Consent Clinical research coordinator Ethics Medical ethics Clinical research
368	Microsoft Word - Site Submission Form Completion Guidelines Version 5, dated August 25, 2008.doc Add to Reading List Source URL: www.harrisonirb.com Language: English - Date: 2013-09-27 19:45:38 Medicine Pharmacology Medical ethics Medical statistics Pharmaceutical industry Food and Drug Administration Informed consent Institutional review board Clinical research coordinator Research Clinical research Health
369	Regulations Only 14 Jun 07 no hyperlinks.pub Add to Reading List Source URL: www.utmb.edu Language: English - Date: 2013-09-19 18:25:20 Science Institutional review board Clinical trial Declaration of Helsinki Investigational New Drug Human subject research Informed consent Clinical research coordinator Public Responsibility in Medicine and Research Clinical research Research Medicine
370	Florida Gulf Coast University Institutional Review Board Office of Research and Graduate Studies Suite 202, Howard Hall[removed] Add to Reading List Source URL: www.fgcu.edu Language: English - Date: 2013-12-18 11:12:08 Research Applied ethics Design of experiments Pharmacology Pharmaceutical industry Institutional review board Informed consent Consent Clinical research coordinator Ethics Clinical research Medical ethics

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