Add to ORKGThis paper proceeds in four parts. Part I. maps the powers of the various branches over the FDA. Part II. describes the Clinton administration’s tobacco regulation. Part III. analyzes the repercussions of the failed lawsuit, and Part IV., the conclusion, peaks at the new Bush administration and suggests reasons why Bush would be wise to adopt Clinton’s style of presidential lawmaking through the FDA (and other agencies) so long as such action has been reasonably delegated to the agency
Political bureaucracies make the overwhelming majority of public policy decisions in the United Stat...
This Article reexamines the role of FDA regulation in motivating investment in biopharmaceutical inn...
Citing agenda-building theory, this article examines the influence of three key factors on the news ...
The Food and Drug Administration never has been and never will be completely insulated from politics...
This paper discusses the history of the FDA with a focus on the expansion of FDA regulatory powers
For most of its existence, the Food and Drug Administration (FDA) has acted as the ultimate arbiter ...
This paper is a study of how the American people interact with and understand a complicated governme...
Assessments of a President’s first 100 days in office typically focus on legislative priorities and ...
The purpose of this article is to provide background about the United States Food and Drug Administr...
This paper seeks (1) to provide the background necessary to understand current commercial speech jur...
Professor Cass Sunstein argues that the FDA has the authority to regulate tobacco products. He consi...
Professor Richard Merrill contends that the Federal Food, Drug, and Cosmetic Act does not grant the ...
Food and Drug Administration (FDA) regulatory reform has become a controversial, politically charged...
Professor Cass Sunstein argues that the FDA has the authority to regulate tobacco products. He consi...
In 2001, a group of private citizens, public health groups, and medical organizations petitioned th...
Political bureaucracies make the overwhelming majority of public policy decisions in the United Stat...
This Article reexamines the role of FDA regulation in motivating investment in biopharmaceutical inn...
Citing agenda-building theory, this article examines the influence of three key factors on the news ...
The Food and Drug Administration never has been and never will be completely insulated from politics...
This paper discusses the history of the FDA with a focus on the expansion of FDA regulatory powers
For most of its existence, the Food and Drug Administration (FDA) has acted as the ultimate arbiter ...
This paper is a study of how the American people interact with and understand a complicated governme...
Assessments of a President’s first 100 days in office typically focus on legislative priorities and ...
The purpose of this article is to provide background about the United States Food and Drug Administr...
This paper seeks (1) to provide the background necessary to understand current commercial speech jur...
Professor Cass Sunstein argues that the FDA has the authority to regulate tobacco products. He consi...
Professor Richard Merrill contends that the Federal Food, Drug, and Cosmetic Act does not grant the ...
Food and Drug Administration (FDA) regulatory reform has become a controversial, politically charged...
Professor Cass Sunstein argues that the FDA has the authority to regulate tobacco products. He consi...
In 2001, a group of private citizens, public health groups, and medical organizations petitioned th...
Political bureaucracies make the overwhelming majority of public policy decisions in the United Stat...
This Article reexamines the role of FDA regulation in motivating investment in biopharmaceutical inn...
Citing agenda-building theory, this article examines the influence of three key factors on the news ...