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U.S. FOOD AND DRUG ADMINISTRATION DUNKIRK ROAD CAMPUS MASTER PLAN Draft Environmental Impact Statement Appendix C Section 106 Consultation June 2021Prepared by:In cooperation with:This page left intentionally

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What is us food and drug?

The U.S. Food and Drug Administration (FDA) is responsible for protecting the public health by ensuring the safety, efficacy, and security of human and veterinary drugs, biological products, medical devices, food, cosmetics, and products that emit radiation.

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Manufacturers, distributors, and importers of FDA-regulated products are typically required to file with the FDA.

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To fill out the necessary forms for FDA regulation, companies must provide detailed information about their products, including ingredients, manufacturing processes, and safety data.

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The purpose of the FDA is to protect and promote public health through the regulation and supervision of various products, including food, drugs, cosmetics, and medical devices.

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Information required may include product labeling, safety data, manufacturing practices, and adverse event reporting.