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Human subject research
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#	Item
141	Self checklist to be used as guide-NOT TO BE SUBMITTED SELF CHECKLIST (STSS.N A. Add to Reading List Source URL: 14.139.60.56 Language: English - Date: 2016-05-10 06:52:02 Medical ethics Clinical research ethics Human subject research Design of experiments Clinical trials Institutional review board Informed consent Consent IEC
142	Protecting Subjects, Preserving Trust, Promoting Progress– Policy and Guidelines for the Oversight of Individual Financial Interests in Human Subjects Research Task Force on Financial Conflicts of Interest Add to Reading List Source URL: ccnmtl.columbia.edu Language: English - Date: 2007-10-05 14:10:00 Clinical research Medical ethics Health research Research ethics Public Responsibility in Medicine and Research Conflict of interest Human subject research Clinical trial Informed consent Funding of science Health informatics Medical research
143	§ 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
144	FIERC Form 2.4 Informed Consent Evaluation Form Food and Nutrition Research Institute Ethics Review Committee Add to Reading List Source URL: www.fnri.dost.gov.ph Language: English - Date: 2016-03-04 07:48:20 Medical ethics Clinical research ethics Clinical research Human subject research Autonomy Informed consent Public Responsibility in Medicine and Research Consent Clinical research coordinator
145	DOC Document Add to Reading List Source URL: humansubjects.stanford.edu Language: English - Date: 2016-04-12 01:21:57 Medical ethics Informed consent Health Insurance Portability and Accountability Act Institutional review board Consent Privacy Right to withdraw Human subject research Medical privacy Clinical research coordinator Privacy for research participants
146	REQUEST FOR CHANGE IN CAMPUS IRB APPROVAL UNIVERSITY of MISSOURI - ROLLA (UMRIRB-2) Review Requested: Amendment ____ Revision ____ Addendum ____ Other ____ This form is not intended to be used for continuing rev Add to Reading List Source URL: irb.mst.edu Language: English* - Date: 2014-01-22 05:22:59 Medical ethics Clinical research ethics Human subject research Design of experiments Institutional review board Consent Informed consent
147	Microsoft Word - SOP - Board Purpose and Function.doc Add to Reading List Source URL: research.missouri.edu Language: English - Date: 2015-07-01 12:40:12 Medical ethics Clinical research ethics Clinical research Design of experiments Research ethics Institutional review board Public Responsibility in Medicine and Research Human subject research Food and Drug Administration IRB Clinical research coordinator Clinical trial
148	Forum for Ethical Review Committees in Asia and the Western Pacific FERCAP NEWSLETTER March 31, 2009 Add to Reading List Source URL: www.fercap-sidcer.org Language: English - Date: 2010-02-19 02:38:03 Clinical research Pharmaceutical industry Medical ethics Design of experiments Institutional review board Tropical disease Human subject research Fudan University Ethics committee Mahidol University Clinical trial Good clinical practice
149	DOC Document Add to Reading List Source URL: www.fye.vt.edu Language: English - Date: 2016-08-17 22:16:21 Medical ethics Human subject research Informed consent Public Responsibility in Medicine and Research Psychology Age of consent Educational technology Consent Question BDSM Evaluation
150	ETHICS IN PSYCHIATRIC RESEARCH Dr. Prathap Tharyan1 1. INTRODUCTION Psychiatric disorders are widely prevalent worldwide. Surveys conducted in developed as well as developing countries have shown that, during their entir Add to Reading List Source URL: www.indianjpsychiatry.org Language: English - Date: 2009-08-19 02:44:20 Medical ethics Clinical research ethics Clinical research Human subject research Research ethics Institutional review board Declaration of Helsinki Public Responsibility in Medicine and Research Clinical trial Good clinical practice Council for International Organizations of Medical Sciences Informed consent

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