- New
-
Topics
- All Categories
- Metaphysics and Epistemology
- Value Theory
- Science, Logic, and Mathematics
- Science, Logic, and Mathematics
- Logic and Philosophy of Logic
- Philosophy of Biology
- Philosophy of Cognitive Science
- Philosophy of Computing and Information
- Philosophy of Mathematics
- Philosophy of Physical Science
- Philosophy of Social Science
- Philosophy of Probability
- General Philosophy of Science
- Philosophy of Science, Misc
- History of Western Philosophy
- Philosophical Traditions
- Philosophy, Misc
- Other Academic Areas
- Journals
- Submit material
- More
Source Data Verification in Clinical Trials Involving the Temporarily Incapacitated Subject: Is There a Missing Link in the Notion of Proxy Consent?
IRB: Ethics & Human Research 14 (4):8 (1992)
Abstract
This article has no associated abstract. (fix it)Other Versions
No versions found
My notes
Similar books and articles
Competing Clinical Trials in the Same Institution: Ethical Issues in Subject Selection and Informed Consent.Elisa J. Gordon & Kenneth C. Micetich - 2002 - IRB: Ethics & Human Research 24 (2):1.
Informed Consent for Alzheimer's Disease Clinical Trials: A Survey of Clinical Investigators.Jason H. T. Karlawish, David Knopman, Christopher M. Clark, John C. Morris, Daniel Marson, Peter J. Whitehouse & Claudia H. Kawas - 2002 - IRB: Ethics & Human Research 24 (5):1.
Subject selection for clinical trials.American Medical Association - 1998 - IRB: Ethics & Human Research 20 (2-3):12.
Subject Selection for Clinical Trials.American Medical Association Council on Ethical and Judicial Affairs - forthcoming - IRB: Ethics & Human Research.
Quebec physicians' knowledge and opinions regarding substitute consent for decisionally incapacitated older adults.Gina Bravo, Marie-France Dubois, Mariane Paquet, Fabienne Langlois & Jean-Pierre Bernier - 2003 - IRB: Ethics & Human Research 26 (5):12-17.
General provisional proxy consent to research: redefining the role of the local research ethics board.Daryl Pullman - 1999 - IRB: Ethics & Human Research 21 (3):1.
Ethical Issues Arising When Interim Data in Clinical Trials Is Restricted to Independent Data Monitoring Committees.Robert J. Wells, Peter S. Gartside & Christine L. McHenry - 2000 - IRB: Ethics & Human Research 22 (1):7.
The Ethical Challenge of Human Research.Franklin G. Miller - 2012 - New York, US: Oxford University Press.
The Changing Clinical Trials Scene: The Role of the IRB.Shiela C. Mitchell & Jay Steingrub - 1988 - IRB: Ethics & Human Research 10 (4):1.
Analytics
Added to PP
2014-03-31
Downloads
96 (#545,543)
6 months
17 (#692,139)
2014-03-31
Downloads
96 (#545,543)
6 months
17 (#692,139)
Historical graph of downloads
Try MATCHA Writer if you're interested in citing directly from PhilPapers and certifying your authorship.
This site uses cookies and Google Analytics (see our terms & conditions for details regarding the privacy implications). Use of this site is subject to terms & conditions.
All rights reserved by The PhilPapers Foundation