Moral Gridlock: Conceptual Barriers to No-Fault Compensation for Injured Research Subjects

Author:

Henry Leslie Meltzer

Abstract

The federal regulations that govern biomedical research, most notably those enshrined in the Common Rule, are a product of their time. Born in the aftermath of wartime atrocities committed by Nazi doctors, and influenced by domestic research scandals like the Willowbrook and Tuskegee studies, the regulations express a protectionist ethos aimed at safeguarding subjects of human experimentation from the potential harms of research participation. Requirements for informed consent, risk minimization, equitable subject selection, and peer review of proposed research rest on the presumption that the research enterprise owes subjects a duty of protection.

Publisher

Cambridge University Press (CUP)

Subject

Health Policy,General Medicine,Issues, ethics and legal aspects

Reference93 articles.

1. 15. Moral Science, supra note 13, at 64; Responsible Research, supra note 11, at 191; Ethical and Policy Issues, supra note 8, at 126; Compensating for Research Injuries, supra note 10, at 103.

2. Justice for Injured Research Subjects

3. 41. Claimants who participated in the Fund waived their right to seek compensation for their claims through the tort system. See ATSSSA, supra note 38, § 405(c)(3)(B)(i), 49 U.S.C. § 40101 note; Schneider v. Feinberg, 345 F.3d 135, 139 (2d Cir. 2003).

4. 71. Id., at VI–9.

5. 23. See Ethically Impossible, supra note 19.

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