The problem of standard of care in clinical research concerns the level of treatment that investigators must provide to subjects in clinical trials. Commentators often formulate answers to this problem by appealing to two distinct types of obligations: professional obligations and natural duties. In this article, I investigate whether investigators also possess institutional obligations that are directly relevant to the problem of standard of care, that is, those obligations a person has because she occupies a particular institutional role. I examine two types of institutional contexts: (1) public research agencies – agencies or departments of states that fund or conduct clinical research in the public interest; and (2) private-for-profit c...
An estimated 2.5 million Americans participate in clinical research annually. Participation exposes...
ii This dissertation research investigates the concept and practices of ethical responsibility in th...
Two sets of federal regulations, the Common Rule and Food and Drug Administration (FDA) regulation...
The problem of standard of care in clinical research concerns the level of treatment that investigat...
When may a physician enroll a patient in clinical research? An adequate answer to this question requ...
Discussions on the ethics and regulation of clinical research have a great deal to say about the res...
One often-overlooked task for applied ethics is to determine not just what must be done, but who sho...
In the research ethics literature, there is strong disagreement about the ethical acceptability of p...
With the expansion of clinical research in developing countries, there is a need to explain obligati...
The article develops fresh perspectives on the normative practice model (npm) by extending its appli...
Heated debate surrounds the question whether the relationship between physician-researcher and patie...
Background: Research codes of conduct offer guidance to researchers with respect to which values sho...
This Article explores the implications for medical care of a debate that is more familiar in the law...
C1 - Journal Articles RefereedBACKGROUND: Although industry sponsors provide approximately 70 percen...
Clinical guidelines are important tools for managing health care quality. Research on the origins of...
An estimated 2.5 million Americans participate in clinical research annually. Participation exposes...
ii This dissertation research investigates the concept and practices of ethical responsibility in th...
Two sets of federal regulations, the Common Rule and Food and Drug Administration (FDA) regulation...
The problem of standard of care in clinical research concerns the level of treatment that investigat...
When may a physician enroll a patient in clinical research? An adequate answer to this question requ...
Discussions on the ethics and regulation of clinical research have a great deal to say about the res...
One often-overlooked task for applied ethics is to determine not just what must be done, but who sho...
In the research ethics literature, there is strong disagreement about the ethical acceptability of p...
With the expansion of clinical research in developing countries, there is a need to explain obligati...
The article develops fresh perspectives on the normative practice model (npm) by extending its appli...
Heated debate surrounds the question whether the relationship between physician-researcher and patie...
Background: Research codes of conduct offer guidance to researchers with respect to which values sho...
This Article explores the implications for medical care of a debate that is more familiar in the law...
C1 - Journal Articles RefereedBACKGROUND: Although industry sponsors provide approximately 70 percen...
Clinical guidelines are important tools for managing health care quality. Research on the origins of...
An estimated 2.5 million Americans participate in clinical research annually. Participation exposes...
ii This dissertation research investigates the concept and practices of ethical responsibility in th...
Two sets of federal regulations, the Common Rule and Food and Drug Administration (FDA) regulation...