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"

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

American Journal of Bioethics: Volume 11 Issue 5 - May 2011

Response to Open Peer Commentaries on ?Social Contexts Influence Ethical Considerations of Research

American Journal of Bioethics: Volume 11 Issue 5 - May 2011

Dealing With the Long-Term Social Implications of Research

American Journal of Bioethics: Volume 11 Issue 5 - May 2011

Social Contexts Influence Ethical Considerations of Research

American Journal of Bioethics: Volume 10 Issue 12 - Dec 2010

Vindication of Prenatal Diagnosis and Treatment of Congenital Adrenal Hyperplasia With Low-Dose Dexamethasone

American Journal of Bioethics: Volume 10 Issue 8 - Aug 2010

Responses to Open Peer Commentaries on ?Research Exceptionalism?

American Journal of Bioethics: Volume 10 Issue 8 - Aug 2010

Research Exceptionalism

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?

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

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News (3)

March 3, 2014 4:08 pm

Women Still Left Out of Medical Research: Report

Two decades after the passage of a landmark law mandating that women be represented in government-funded medical research, a new report reveals that the world of science is still ignoring women’s unique health issues far more than it should.

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.