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FDA and Health Canada are regulatory agencies responsible for safeguarding publics health and safety. Their operations are governed by separate legislative systems. While Health Canada is part of the Canadian federal government, the FDA is division of the Department of Health and Human Services in the United States.
The federal regulation of food, drugs, cosmetics, biologics, medical products and tobacco is legally mandated by acts of the United States Congress.
The United States Food and Drug Administration (FDA or US FDA) is a federal agency of the Department of Health and Human Services.
The FDCA authorizes the FDA with the following tasks, among many others: Mandate drug manufacturers to submit evidence of new drugs safety and effectiveness before marketing and distribution to the general public. Issue and enforce quality standards for food, drugs, medical devices, and cosmetics.
The Food and Drug Administration conducts objective economic analyses of all important proposed and final regulations, which includes the Regulatory Impact Analysis (RIA) as well as other analyses mandated by various statutes and executive orders.
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Aside from overseeing the meat, poultry, eggs, and produce, the USDA also handles the agencies responsible for US dietary guidelines and Supplemental Nutrition Assistance Program (SNAP) benefits. Meanwhile, the FDA regulates the nutrition facts labels on all processed food.
FDA, an agency within the U.S. Department of Health and Human Services, protects public health by regulating human and veterinary drugs, vaccines and other biological products, medical devices, our nations food supply, cosmetics, dietary supplements, electronic radiation emitting products, and tobacco products.
To support its public health activities, the FDA relies on (1) annual funding that Congress provides for the agency, and (2) user fees paid by industries that make and market FDA-regulated products, and user fees paid by certain other entities.

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