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Informed consent
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101	WORLD MEDICAL ASSOCIATION DECLARATION OF HELSINKI Ethical Principles for Medical Research Involving Human Subjects Adopted by the 18th WMA General Assembly, Helsinki, Finland, June 1964, and amended by the: 29th WMA Gene Add to Reading List Source URL: irb.sinica.edu.tw Language: English - Date: 2009-01-10 02:29:53 Medical research Medicine Medical ethics Research Clinical research ethics Clinical research Research ethics Declaration of Helsinki Informed consent Institutional review board Clinical trial Human subject research
102	Instructions Questions? Contact the IRB Education Specialist atSee guidance GUI-6 and HRPP Policy Manual Chapter 5.9. Report to IRB The protocol director must submit the following to the IRB within five ( Add to Reading List Source URL: humansubjects.stanford.edu Language: English - Date: 2016-04-12 01:21:50 Medical research Medical ethics Research Health Autonomy Clinical research ethics Food and Drug Administration Informed consent Expanded access Investigational New Drug Consent Clinical trial
103	GUIDING ETHICAL PRINCIPLES Preamble In our endeavours to achieve international recognition as the peak reference group for all matters associated with human sexuality, the World Association for Sexual Health (WAS) and t Add to Reading List Source URL: www.europeansexology.com Language: English - Date: 2012-09-06 10:41:08 Applied ethics Research Clinical research ethics Ethics Medical ethics Medical research Professional ethics Health World Association for Sexual Health Confidentiality Informed consent Declaration of Helsinki
104	PDF Document Add to Reading List Source URL: www.dcya.gov.ie Language: English - Date: 2012-04-19 10:29:48 Medical research Applied ethics Clinical research ethics Medical ethics Research Clinical research Human subject research Design of experiments Informed consent Public Responsibility in Medicine and Research Institutional review board Research ethics
105	C O P E CO M M ITTE E ON P U B LICATI ON ETH ICS What to do if you suspect an ethical problem with a submitted manuscript Reviewer (or editor) raises ethical Add to Reading List Source URL: publicationethics.org Language: English - Date: 2015-05-25 02:46:06 Clinical research ethics Human subject research Medical ethics Informed consent Research Ethics Medicine
106	Microsoft Word - SOP - Informed Consent - Process and Issues.doc Add to Reading List Source URL: research.missouri.edu Language: English - Date: 2015-07-01 12:44:04 Medical ethics Medical research Clinical research ethics Ethics Applied ethics Human subject research Autonomy Design of experiments Informed consent Institutional review board Consent Age of consent
107	Page 1 ofSUMMER CAMP REGISTRATION FORM ARTS, FITNESS & ADVENTURE, COMMUNITY EDUCATION CENTER Add to Reading List Source URL: www.oneidanationarts.org Language: English - Date: 2016-04-20 16:01:33 Clinical research ethics Human subject research Informed consent Boy Scouting Research Ethics Science
108	ORGANIZATION INFO MOB Report NIAID, DIVISION OF AIDS, MONITORING OPERATIONS BRANCH Add to Reading List Source URL: www.hanc.info Language: English - Date: 2016-07-28 14:18:32 Medical research Health Medical ethics Clinical research Design of experiments Human subject research Clinical trial Informed consent Institutional review board Ic HIV Vaccine Trials Network Clinical research associate
109	Appendix IV Participant Information Sheet and Consent Form (TCS) Add to Reading List Source URL: www.psy.ed.ac.uk Language: English - Date: 2015-03-09 11:25:31 Experimental psychology Survey methodology Medical ethics Philosophy of education Debriefing Experiential learning Research Informed consent Interview Psychology Questionnaire Science
110	Microsoft Word - SOP - Informed Consent - Types and Elements.doc Add to Reading List Source URL: research.missouri.edu Language: English - Date: 2015-07-01 12:44:32 Medical research Medical ethics Research Applied ethics Clinical research ethics Clinical research Pharmaceutical industry Human subject research Institutional review board Informed consent Clinical trial Investigational device exemption

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