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Research ethics
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371	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
372	DOWNLOAD COVERSHEET: This is a standard advance directive for your state, made available to you as a courtesy by Lifecare Directives, LLC. You should be aware that extensive research has demonstrated that there are sign Add to Reading List Source URL: www.lifecaredirectives.com Language: English - Date: 2010-04-17 19:56:18 Health law Legal documents Medical ethics Euthanasia Medical law Advance healthcare directive Power of attorney Healthcare proxy Five Wishes Surrogate decision-maker
373	FIERC Form 1.2 Curriculum Vitae Food and Nutrition Research Institute Ethics Review Committee Add to Reading List Source URL: www.fnri.dost.gov.ph - Date: 2016-03-04 07:48:19
374	79 Defining the Scope of the Problem Informed Consent and Deception in Add to Reading List Source URL: www.minesandassociates.com Language: English - Date: 2016-01-02 13:48:00 Medical ethics Clinical research ethics Research ethics Autonomy Clinical research Informed consent Public Responsibility in Medicine and Research Deception Declaration of Helsinki Counseling psychology Human subject research Psychology
375	DOWNLOAD COVERSHEET: This is a standard advance directive for your state, made available to you as a courtesy by Lifecare Directives, LLC. You should be aware that extensive research has demonstrated that there are sign Add to Reading List Source URL: www.lifecaredirectives.com Language: English - Date: 2010-04-17 19:56:42 Health law Legal documents Medical ethics Euthanasia Medical law Advance healthcare directive Power of attorney Healthcare proxy Advance care planning Surrogate decision-maker
376	Office of the Vice-President, Research and Innovation Office of Research Ethics Add to Reading List Source URL: www.research.utoronto.ca Language: English - Date: 2016-05-16 14:45:05 Medical ethics Clinical research ethics Human subject research Professional ethics Pharmaceutical industry Research ethics Clinical research coordinator Informed consent Psychology Consent Ethics Debriefing
377	Stanford University HRPP Guidance General Requirements for Informed Consent Add to Reading List Source URL: researchcompliance.stanford.edu Language: English - Date: 2016-04-12 01:21:52 Clinical research Medical ethics Pharmaceutical industry Research ethics Clinical research coordinator Clinical trial Informed consent Human subject research
378	Moral preferences Francesca Rossi IBM T.J. Watson Research center∗ 1 Add to Reading List Source URL: intelligence.org Language: English - Date: 2016-05-16 16:40:19 Social philosophy Normative ethics Ethics Philosophy of life Meta-ethics Preference Morality Consequentialism Artificial intelligence Good and evil Virtue ethics
379	SHIP Public Engagement: Summary of Focus Group Findings Introduction The Scottish Health Informatics Programme (SHIP) is a Scotland-wide research and development initiative exploring ways of managing and analysing Electr Add to Reading List Source URL: www.scot-ship.ac.uk Language: English - Date: 2014-04-01 08:15:28 Qualitative research Health informatics Medical technology Research ethics Data sharing Focus group National Health Service Medical privacy Patient Information Advisory Group
380	Nationally Accredited Essential Human Research Ethics Committee (HREC) Training Course PRAXIS Australia provides a rich array of Add to Reading List Source URL: www.praxisaustralia.com.au Language: English Ethics committee Praxis

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