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Direct-to-Consumer Advertising of Prescription Drugs

Description: The Direct-to-Consumer advertising of perscription drugs by pharmaceutical companies has been described as any promotional effort with respect to these drugs that targets the general public through the lay media. This report contains information on growth in spending on direct-to-consumer prescription drug advertising, the impact of such advertising, the FDA's existing authority to regulate such advertising, funding, and legislative issues.
Date: March 25, 2005
Creator: Vogt, Donna U.
Partner: UNT Libraries Government Documents Department
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Food Safety Issues in the 106th Congress

Description: The Centers for Disease Control and Prevention (CDC) released in September new estimates showing that each year in the United States 76 million people get sick, 325,000 are hospitalized, and 5,000 die from food-related illnesses. Food-borne illness is a serious public health problem. Often, people do not seek medical help and their illness is not officially reported. Yet, consumers have become aware of the serious consequences of illnesses linked to a growing variety of foods, produced domestic… more
Date: November 7, 2000
Creator: Vogt, Donna U.
Partner: UNT Libraries Government Documents Department
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The Delaney Dilemma: Regulating Pesticide Residues in Foods -- Seminar Proceedings, March 16, 1993

Description: A provision in the Federal Food, Drug, and Cosmetic Act, the Delaney Clause, appears to lower risks in the setting of tolerances for pesticide residues. It prohibits any substance from being added to processed foods if it induces cancer in man or animals. In reality, the provision created a dilemma because the zero-risk statute makes it difficult to regulate pesticides. Because of the prescription of Delaney, tolerances (legal limits) are established differently for carcinogens and non-carcinog… more
Date: May 19, 1993
Creator: Vogt, Donna U.
Partner: UNT Libraries Government Documents Department
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Food Additive Regulations: A Chronology

Description: The 104th Congress is actively debating proposals to reform several aspects of the Food and Drug Administration's (FDA) process for regulating consumer products, including its approval process for food additives. In June 1995, the Food and Drug Administration (FDA) announced at a House Government Reform and Oversight Subcommittee hearing several policy shifts in its food additive pre-market approval process which will soon be implemented.
Date: September 13, 1995
Creator: Vogt, Donna U.
Partner: UNT Libraries Government Documents Department
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The Delaney Clause: The Dilemma of Regulating Health Risk for Pesticide Residues

Description: Under the authority of the Federal Food, Drug, and Cosmetic Act (FFDCA), the Environmental Protection Agency (EPA) is responsible for establishing tolerances for pesticide residues in or on foods and feeds. Tolerances are legal limits to the amount of pesticide residues that can be found on a raw agricultural commodity at the farm gate or in a processed food. The FFDCA has two sections, 408 and 409, which set up different and inconsistent criteria for setting tolerances for pesticide residues i… more
Date: November 9, 1992
Creator: Vogt, Donna U.
Partner: UNT Libraries Government Documents Department
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Food Safety Issues in the 107th Congress

Description: This report gives an overview of food safety issues in the 107th Congress. It briefly discusses the president's several food safety initiatives and describes requested resources for federal funding and for cooperation among federal agencies involved in food safety activities.
Date: November 7, 2001
Creator: Vogt, Donna U.
Partner: UNT Libraries Government Documents Department
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Labeling of Genetically Modified Foods

Description: This report focuses on views surrounding the labeling of genetically modified (GM) foods in consideration of the Food and Drug Administration's (FDA) draft guidance for industry on voluntary efforts to label GM foods in 2001 following its GM food labeling policy of May 1992.
Date: January 18, 2001
Creator: Vogt, Donna U.
Partner: UNT Libraries Government Documents Department
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Importing Prescription Drugs: Objectives, Options, and Outlook

Description: This report provides an overview about the Objectives, Options, and Outlook on Importing Prescription Drugs.it also examines the issues,spells out how they are treated from bill to bill, and refer to alternatives to important to ease the burden of prescription drug.
Date: December 8, 2005
Creator: Thaul, Susan & Vogt, Donna U.
Partner: UNT Libraries Government Documents Department
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Food Biotechnology in the United States: Science, Regulation, and Issues

Description: This report provides basic information on the science of food biotechnology. It discusses regulatory policies and issues of concern about the use of biotechnology to modify foods through genetic engineering. It describes the scientific processes used and current products available. It explains how all three major federal agencies - the Food and Drug Administration, the U.S. Department of Agriculture, and the Environmental Protection Agency - regulate these foods.
Date: June 2, 1999
Creator: Vogt, Donna U. & Parish, Mickey
Partner: UNT Libraries Government Documents Department
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Food Biotechnology in the United States: Science, Regulation, and Issues

Description: This report discusses the science of food biotechnology, and the federal structure by which it is regulated. Because U.S. farmers are adopting this technology at a rapid rate, some observers advocate a more active role for the federal government to ensure that farmers have equal access to this technology. Others believe that federal officials should play a more active role in protecting the environment, funding more research, and participating in international trade negotiations to ensure that … more
Date: January 19, 2001
Creator: Vogt, Donna U. & Parish, Mickey
Partner: UNT Libraries Government Documents Department
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