Debate over floors versus ceilings was, until recently, largely hypothetical, due to the rarity of federal imposition of ceilings. During the past year, however, in settings ranging from …
In the preamble to its January 2006 prescription drug labeling rule, the Food and Drug Administration (FDA) asserted that" FDA approval of labeling under the act.. preempts …
This Article takes as its starting point the" agency reference model" for judicial preemption decisions, adopting the foundational premise that courts should take advantage of what …
I. Introduction Although assisted reproductive technologies (ARTs) raise a host of important ethical, legal, and social issues, much of the recent debate has focused on their connection …
By some accounts, we have transitioned to a" knowledge-based" economy dominated by providers and users of various information technologies. 3 Undoubtedly, some sectors of …
The common law of torts is widely considered to be in conflict with the modern regulatory state. Tort law interacts with regulations and their enabling statutes in different ways that are …
Occasionally, one hears the complaint that jurors in civil cases intentionally ignore their instructions and return verdicts inconsistent with the applicable law. 2 Jury nullification has a …
This Article addresses the controversy over the abortifacient drug mifepristone (RU-486). First, it traces the history of the United States Food and Drug Administration's review and …
L Noah - Brooklyn Law Review, 2009 - papers.ssrn.com
This paper attempts to offer a comprehensive evaluation of the various facets of the Products Liability Restatement that relate to medical technologies, and it does so from a perspective …