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Medical ethics
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231	UNM IRB PROTOCOL TITLE: Text VERSION DATE: Text INVESTIGATOR/RESPONSIBLE Text FACULTY: STUDENT INVESTIGATOR: Text Add to Reading List Source URL: cancer.unm-intranet.com Language: English - Date: 2014-10-07 17:53:04 Medical research Medical ethics Research Health care Autonomy Clinical research Pharmaceutical industry Clinical research coordinator Public Responsibility in Medicine and Research Health Insurance Portability and Accountability Act Informed consent Medical privacy
232	Mental Health Tribunal Service Charter The Mental Health Tribunal (Tribunal) is an independent statutory tribunal established under the Mental Health ActThe Tribunal is an essential safeguard under the Act to prot Add to Reading List Source URL: www.mht.vic.gov.au Language: English - Date: 2016-04-10 23:45:15 Psychiatry Medical ethics Mental health law Health Human rights Medicine Mental health Mental health tribunal Tribunal Mental disorder Mental Health Review Tribunal
233	Stericycle Logo_Bedford Sign Only-White Add to Reading List Source URL: www.stericycle.com Language: English - Date: 2015-10-28 13:53:29 Stericycle Biological hazards Medical ethics Biology Waste Pollution Business
234	Phil. Trans. R. Soc. B, 1781–1782 doi:rstbPreface In 1969, William McGuire described the three stages of what he called the life history of an artefact [1]. Add to Reading List Source URL: brainmindhealing.org Language: English - Date: 2016-02-22 11:57:40 Medicine Health care Health Mindbody interventions Clinical research Medical ethics Somatic psychology Learning Placebo Psychoneuroimmunology Classical conditioning Nocebo
235	SAMPLE TRINITY COLLEGE DUBLIN INFORMATION SHEET FOR PARTICIPANTS This sheet should inform participants of the following, as appropriate to the study: • Add to Reading List Source URL: ahss.tcd.ie Language: English - Date: 2014-07-17 07:54:22 Research ethics Medical ethics Experimental psychology Applied ethics Debriefing Experiential learning Right to withdraw Research Science
236	AUTHORIZATION TO USE OR DISCLOSE HEALTH INFORMATION Patient Name: __________________________ Date of Birth: ___________ Medical Record #: __________________ 1. I hereby authorize the UNM Health Sciences Center to disclos Add to Reading List Source URL: hospitals.unm.edu Language: English - Date: 2016-01-11 17:37:08 Health informatics Medical record Health Healthcare quality Patient safety Personal life Medical ethics
237	Advance Directives Informed Decision Making How can a person plan for a time when he Add to Reading List Source URL: hscethics.unm.edu Language: English - Date: 2015-09-09 14:00:43 Medicine Health care Health Medical ethics Ethics Euthanasia Health informatics Medical research Advance healthcare directive Bioethics Resources for clinical ethics consultation Surrogate decision-maker
238	[Code of Federal Regulations] [Title 42, Volume 1] [Revised as of October 1, 2002] From the U.S. Government Printing Office via GPO Access [CITE: 42CFR2.1] Add to Reading List Source URL: www.methadone.org Language: English - Date: 2013-05-14 11:49:51 Health informatics Health Medical record Confidentiality Abuse Applied ethics Patient Safety and Quality Improvement Act Radiation Control for Health and Safety Act
239	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
240	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

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