Nonbeneficial research with individuals who cannot consent: is it ethically better to enroll healthy or affected individuals?

IRB: Ethics & Human Research 25 (4):1-4 (2002)
  Copy   BIBTEX

Abstract

This article has no associated abstract. (fix it)

Links

PhilArchive



    Upload a copy of this work     Papers currently archived: 91,349

External links

Setup an account with your affiliations in order to access resources via your University's proxy server

Through your library

Similar books and articles

What we worry about when we worry about the ethics of clinical research.David Wendler - 2011 - Theoretical Medicine and Bioethics 32 (3):161-180.
Informed consent and genetic information.O. O'Neill - 2001 - Studies in History and Philosophy of Science Part C: Studies in History and Philosophy of Biological and Biomedical Sciences 32 (4):689-704.

Analytics

Added to PP
2014-03-18

Downloads
15 (#923,100)

6 months
3 (#992,474)

Historical graph of downloads
How can I increase my downloads?

Citations of this work

Law & Bioethics: From Values to Violence.Susan M. Wolf - 2004 - Journal of Law, Medicine and Ethics 32 (2):293-306.

Add more citations

References found in this work

No references found.

Add more references