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Clinical trials in brain tumours- What you always wanted to know but were afraid to ask Zarnie Lwin Department of Medical Oncology, Mater Adult Hospital
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Ethical Issues Raised by Current Research on Drug Addiction Dr Tom Walker Centre for Professional Ethics Keele University United Kingdom
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Ethical Legal/Issues in Human Subject Research II ISD II – Infectious Diseases Barbara Barrowman Andrew Latus March 7, 2003
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Ethical Decision-Making in Pediatrics Holly K. Tabor, Ph.D. Assistant Professor Department of Pediatrics University of Washington Treuman Katz Center for
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“Good Clinical Practices” in Meeting Regulatory Responsibilities Terry VandenBosch, RN, PhD, CIP, CCRP Senior Research Compliance Associate Office of Human
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Determining capacity and protecting subjects who have lost capacity Jason Karlawish, MD University of Pennsylvania
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Pre-randomisation consent (Zelen’s method). Background Most individually randomised trials ask patient CONSENT before randomisation. There are problems
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What makes research ethical? 6. Informed consent cont’d Researchers can promote participants’ freedom by: –Adequate assessment of the specific vulnerability
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Legislation in the ED Peer Support 27_01_2015 Sophie Rozwadowski & Kate Myler
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Informed Consent: Requirements
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+ Approaches to consent in children’s emergency care: CONNECT study guidance development @CONNECTStudy
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Consenting for Planet-2
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