Tag: human subjects research
Published Articles (13)
American Journal of Bioethics: Volume 11 Issue 6 - Jun 2011
Response to Open Peer Commentaries on ?Relative Versus Absolute Standards for Everyday Risk in Adolescent HIV Prevention Trials: Expanding the Debate" Jeremy Snyder
American Journal of Bioethics: Volume 11 Issue 6 - Jun 2011
Relative Versus Absolute Standards for Everyday Risk in Adolescent HIV Prevention Trials: Expanding the Debate Jeremy Snyder
American Journal of Bioethics: Volume 11 Issue 5 - May 2011
Response to Open Peer Commentaries on ?Social Contexts Influence Ethical Considerations of Research Robert J. Levine
American Journal of Bioethics: Volume 11 Issue 5 - May 2011
Dealing With the Long-Term Social Implications of Research Alan Fleischman
American Journal of Bioethics: Volume 11 Issue 5 - May 2011
Social Contexts Influence Ethical Considerations of Research Judith Gordon
American Journal of Bioethics: Volume 10 Issue 12 - Dec 2010
Vindication of Prenatal Diagnosis and Treatment of Congenital Adrenal Hyperplasia With Low-Dose Dexamethasone Maria New
American Journal of Bioethics: Volume 10 Issue 8 - Aug 2010
Responses to Open Peer Commentaries on ?Research Exceptionalism? David Hunter
American Journal of Bioethics: Volume 10 Issue 8 - Aug 2010
Research Exceptionalism James Wilson
American Journal of Bioethics: Volume 10 Issue 9 - Sep 2010
The Intellectual and Moral Integrity of Bioethics: Response to Commentaries on ?A Case Study in Unethical Transgressive Bioethics: 'Letter of Concern from Bioethicists' About the Prenatal Administration of Dexamethasone? Laurence B. McCullough
American Journal of Bioethics: Volume 10 Issue 9 - Sep 2010
A Case Study in Unethical Transgressive Bioethics: Letter of Concern from Bioethicists About the Prenatal Administration of Dexamethasone Laurence B. McCullough
News (2)
April 5, 2012 12:57 pm
Your data are not a product (Nature)
The Portable Legal Consent for Common Genomics Research (PLC-CGR) is an experimental bioethics protocol that provides maximum utility to researchers who agree to its terms and protection for the de-identified personal and genomic data volunteered by informed research subjects. Data and resulting publications from this protocol are equally available to all academic, nonprofit and commercial competitors, so that intellectual property claims should arise only on new discoveries based on the data.
April 2, 2012 9:21 am
Grady urges reform in human research (Duke Chronicle)
The way clinical studies inform patients about what they are getting involved with works no better in the U.S. than elsewhere in the world, one expert said. Patients from both developed and third world countries exhibited a similar lack of understanding of the medical research process, which limits their discernible rights, said Christine Grady, the chief of the department of bioethics at the National Institutes of Health Clinical Center.