Zobrazeno 1 - 10
of 45
pro vyhledávání: '"Clark Nardinelli"'
Autor:
Rosemarie L. Summers, Dallas W. Wood, Nellie Lew, Shawn A. Karns, Mary K. Muth, Clark Nardinelli, Janet G. Peckham, Carolyn Wolff
Publikováno v:
Journal of Benefit-Cost Analysis. 13:34-56
Partial equilibrium models have been used extensively by policy makers to prospectively determine the consequences of government programs that affect consumer incomes or the prices consumers pay. However, these models have not previously been used to
Autor:
Clark Nardinelli, Elizabeth R. Botkins, Aaron Kearsley, Nellie Lew, Carolyn Wolff, Bern Caudill Dealy
Publikováno v:
Applied Economics. 53:1112-1126
Pharmacists dispense prescription drugs with leaflets containing information about the specific medication a patient receives. These leaflets vary in format, length, content, and readability for th...
Publikováno v:
The Quarterly Review of Economics and Finance. 67:219-226
The US Food and Drug Administration offers multiple designations for drugs under development, such as the fast-track designation (for drugs that treat serious conditions with unmet medical need) and the orphan drug designation (for drugs that treat r
Publikováno v:
Journal of Benefit-Cost Analysis. 9:496-518
Food and Drug Administration (FDA) published a final regulation in 2004 that requires pharmaceutical manufacturers to place linear bar codes on certain human drug and biological products. The intent was that bar codes would be part of a system where
Autor:
Clark Nardinelli
Publikováno v:
Journal of Benefit-Cost Analysis. 9:519-530
Practitioners of benefit-cost analysis face many difficulties. Despite the best training, guidance, and intentions, practitioners can stumble: actual benefit-cost analysis is hard and mistakes get made. Over the years, I have collected the mistakes I
Publikováno v:
Managerial and Decision Economics. 38:581-594
Pharmaceutical firms are reluctant to disclose proprietary information about a drug's likelihood of approval by the U.S. Food and Drug Administration (FDA) for fear of losing their competitive advantage. Instead, firms may use signals, like the FDA f
Publikováno v:
Risk Analysis. 35:1125-1139
We present an economic welfare-based method to estimate the health costs associated with foodborne illness caused by known viruses, bacteria, parasites, allergens, two marine biotoxins, and unspecified agents. The method generates health costs measur
Publikováno v:
Drug Saf
INTRODUCTION: An important goal in drug regulation is understanding serious safety issues with new drugs as soon as possible. Achieving this goal requires us to understand whether information provided during the Food and Drug Administration (FDA) dru
Publikováno v:
Health Economics. 24:617-624
For products such as tobacco and junk food, where policy interventions are often designed to decrease consumption, affected consumers gain utility from improvements in lifetime health and longevity but also lose utility associated with the activity o
Publikováno v:
Medical Care. 50:987-992
The Food and Drug Administration (FDA) issued a Public Health Advisory entitled "Suicidal Thinking in Children and Adolescents Being Treated with Strattera (Atomoxetine)" on September 29, 2005. At FDA's request, the manufacturer subsequently added a