Add to ORKGFor over 40 years, the Food and Drug Administration has been collecting evidence that the routine administration of antibiotics to animals destined for the food supply contributes to the development of antibiotic-resistant infections in the human population. For all these years, the FDA has put off acting with any force on this health risk. The agency’s explanation has been that the Food, Drug and Cosmetic Act requires it to hold time- and resource-intensive formal hearings before it can withdraw approvals for antibiotics used for the purposes of promoting growth and preventing infection in food animals. In so arguing, the FDA has ignored decades of developments in administrative law and has misread its own statute. The FDA has the discreti...
This article explores the legality and wisdom of the FDA’s effort to persuade courts to find most fa...
The Delaney Clause, the most famous federal health statute, bars Food and Drug Administration (FDA) ...
In many critical industries, the Food and Drug Administration’s (FDA’s) marketing authorization deci...
For over 40 years, the Food and Drug Administration has been collecting evidence that the routine ad...
In 1977, the Food and Drug Administration initiated a process to withdraw approval of the subtherape...
For most of its existence, the Food and Drug Administration (FDA) has acted as the ultimate arbiter ...
For much of the last half-century, the Food and Drug Administration has earned a reputation as one o...
Private party oversight has proven to be ineffective at countering inaction by the Food and Drug Adm...
In January 2018, Scott Gottlieb, the Commissioner of the US Food and Drug Administration (FDA), stat...
In the twentieth century, the Food and Drug Administration (“FDA”) rose to prominence as a respected...
he world is struggling to deal with antibiotic resistance emanating from the large-scale use of anti...
A letter report issued by the Government Accountability Office with an abstract that begins "Antibio...
Testimony issued by the Government Accountability Office with an abstract that begins "The Food and ...
There have been considerable charges and counter-charges the United States Food and Drug Administra...
The Food and Drug Administration (FDA) has developed an informal framework for regulating press rele...
This article explores the legality and wisdom of the FDA’s effort to persuade courts to find most fa...
The Delaney Clause, the most famous federal health statute, bars Food and Drug Administration (FDA) ...
In many critical industries, the Food and Drug Administration’s (FDA’s) marketing authorization deci...
For over 40 years, the Food and Drug Administration has been collecting evidence that the routine ad...
In 1977, the Food and Drug Administration initiated a process to withdraw approval of the subtherape...
For most of its existence, the Food and Drug Administration (FDA) has acted as the ultimate arbiter ...
For much of the last half-century, the Food and Drug Administration has earned a reputation as one o...
Private party oversight has proven to be ineffective at countering inaction by the Food and Drug Adm...
In January 2018, Scott Gottlieb, the Commissioner of the US Food and Drug Administration (FDA), stat...
In the twentieth century, the Food and Drug Administration (“FDA”) rose to prominence as a respected...
he world is struggling to deal with antibiotic resistance emanating from the large-scale use of anti...
A letter report issued by the Government Accountability Office with an abstract that begins "Antibio...
Testimony issued by the Government Accountability Office with an abstract that begins "The Food and ...
There have been considerable charges and counter-charges the United States Food and Drug Administra...
The Food and Drug Administration (FDA) has developed an informal framework for regulating press rele...
This article explores the legality and wisdom of the FDA’s effort to persuade courts to find most fa...
The Delaney Clause, the most famous federal health statute, bars Food and Drug Administration (FDA) ...
In many critical industries, the Food and Drug Administration’s (FDA’s) marketing authorization deci...