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Hazardous to Our Health? (FDA Regulation of Health Care Products)
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Product Details
Author:
Robert Higgs, Joel J. Nobel
Format:
Paperback
Pages:
113
Publisher:
Independent Institute (February 1, 1995)
Imprint:
Independent Institute
Language:
English
ISBN-13:
9780945999416
ISBN-10:
0945999410
Weight:
6.4oz
Dimensions:
6" x 9" x 0.2"
File:
Eloquence-SimonSchuster_04022026_P9912986_onix30_Complete-20260402.xml
Folder:
Eloquence
List Price:
$14.95
Pub Discount:
65
Case Pack:
48
As low as:
$11.51
Publisher Identifier:
P-SS
Discount Code:
A
Overview
The Food and Drug Administration (FDA) is one of the most powerful of federal regulatory agencies, if not the most powerful. It regulates over 25% of all consumer goods sold in the United States. It makes decisions on a daily basis that affect the lives of millions of people.
While the FDA was created to protect the public, how well is it fulfilling this mission and whose interests is it actually protecting?
In this book, four outstanding scholars examine how the FDA accumulated its enormous power and what effects it has had on the public. It also explores who actually benefits and loses from FDA actions, and whether alternatives exist to safeguard the health of Americans. This book raises serious questions about the wisdom of giving policing power with little oversight or appeal process to scientists, as the FDA currently does. It also argues forcefully that the FDA unnecessarily delays beneficial medicines and medical devices, many of which are routinely available in Europe, from being available to Americans.
While the FDA was created to protect the public, how well is it fulfilling this mission and whose interests is it actually protecting?
In this book, four outstanding scholars examine how the FDA accumulated its enormous power and what effects it has had on the public. It also explores who actually benefits and loses from FDA actions, and whether alternatives exist to safeguard the health of Americans. This book raises serious questions about the wisdom of giving policing power with little oversight or appeal process to scientists, as the FDA currently does. It also argues forcefully that the FDA unnecessarily delays beneficial medicines and medical devices, many of which are routinely available in Europe, from being available to Americans.
