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Informed consent
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#	Item
131	CHK-3n IRB NON-MED Reviewer Checklist FORM Add to Reading List Source URL: humansubjects.stanford.edu Language: English - Date: 2016-04-12 01:21:51 Medical ethics Medical research Clinical research ethics Autonomy Applied ethics Ethics Human subject research Informed consent Consent Institutional review board
132	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
133	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
134	ANNEX 2 Form AFAPPLICATION FORM for RESUBMITTED PROTOCOL REVIEW Protocol Number (To be assigned by REBH member secretary): ... Protocol Title: ... Add to Reading List Source URL: www.health.gov.bt Language: English - Date: 2016-07-05 05:03:16 Medical research Clinical research Pharmaceutical industry Clinical trials Medical ethics Informed consent Principal investigator Clinical research coordinator
135	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
136	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
137	Version Date: Version Date: September 2015 © Horizon Health Network - Ethics Services Internal Working Document Page 2 of 10 Horizon Health Network Research Ethics Board Add to Reading List Source URL: en.horizonnb.ca Language: English - Date: 2015-10-08 09:05:45 Medical research Pharmaceutical industry Clinical research Clinical research coordinator Clinical trial Informed consent Confidentiality Good clinical practice Medical privacy
138	http://www.e-affect.com/aaahc-email/email-7-16/email.html Add to Reading List Source URL: www.aaahc.org Language: English - Date: 2016-07-06 16:10:18 Medical ethics Healthcare quality Accreditation Accreditation Association for Ambulatory Health Care Medical terminology Informed consent Consent Patient Medicine Public Responsibility in Medicine and Research Surgery Medical home
139	Microsoft Word - Indigenous Peoples and Climate Change - Ready for Publication.doc Add to Reading List Source URL: no-redd.com Language: English - Date: 2015-09-03 00:49:45 United Nations Framework Convention on Climate Change Carbon finance Climate change mitigation Climate change Adaptation to global warming Kyoto Protocol Clean Development Mechanism Reducing emissions from deforestation and forest degradation Free prior and informed consent
140	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

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