Abstract In the United States, the Food and Drug Administration (FDA) provides public
oversight of the safety and efficacy of drugs; medical devices; biologics like vaccines and …

The US Food and drug Administration (FDA) is estimated to regulate markets accounting for
about 20% of consumer spending in the US. This paper proposes a general methodology to …

The US Food and Drug Administration (FDA) is estimated to regulate markets accounting for
about 20% of consumer spending in the US Despite the FDA's strict adherence to evidence …

Responding to certain drug-related public health disasters, Congress spent the greater part
of the twentieth century increasing the amount of regulation imposed on pharma ceutical …

Historically, profitability, market shares, and potential government regulatory hur dles have
been the crucial factors utilized by companies when evaluating and devel oping possible …

This paper examines the arguments for changing the ways that UK drug prices are
regulated. In the UK, NHS pharmaceutical expenditures on branded drugs, currently worth …

The Food and Drug Administration regulates drug approvals to increase public health by
keeping unsafe and ineffective drugs off the market while allowing pharmaceutical firms to …

On October 6, 1992, the US House of Representatives passed HR 6181, which includes the
Prescription Drug User Fee Act of 1992. The Senate passed the bill the next day, and the …

Food, Drug, and. Cosmetic Act''has produced from time to time a demand that regulators
consider the economic consequences of the actions they take to protect the public health …

IT is a commonplace of life in the developed world that consumers are required to secure the
advice and permission of a physician before they may consume certain drugs. It was not …