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Downstream Effects of Class of Trade ImplicationsPresented by Stephanie Trunk Partner Aren't Fox Washington, DC New York, NY Los Angeles, Cajuns 21, 2017Presentation Overview Approach to Classifying
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The Food and Drug Administration (FDA) is a federal agency responsible for regulating and supervising the safety and efficacy of food, drugs, medical devices, vaccines, cosmetics, and other products.
Various companies and organizations involved in the manufacturing, distribution, and sale of food, drugs, medical devices, vaccines, and cosmetics are required to file with the FDA as per regulatory requirements.
Filing out the necessary forms, providing accurate information about the product, conducting required tests and studies, and ensuring compliance with FDA regulations are some of the steps involved in filling out the FDA submissions.
The primary purpose of the FDA is to protect public health by ensuring the safety and efficacy of food, drugs, medical devices, vaccines, cosmetics, and other products available to consumers.
Information such as product formulation, manufacturing process, labeling, safety data, clinical trial results, adverse event reports, and regulatory status must be reported on FDA submissions.
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