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Food and Drug Administration Advisory Committee Member
Acknowledgment of Financial Interests
Name of Advisory Committee Member: Nicole R. Gonzales, M.D.
Committee: Neurological Devices Panel of the
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What is food and drug administration?
Food and Drug Administration (FDA) is a federal agency in the United States responsible for regulating and supervising the safety of food, dietary supplements, prescription and over-the-counter medications, vaccines, biopharmaceuticals, blood transfusions, medical devices, electromagnetic radiation emitting devices, and veterinary products.
Who is required to file food and drug administration?
Manufacturers, distributors, importers, and other entities involved in the production and distribution of food, drugs, and medical products are required to file with the FDA.
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To fill out FDA forms, companies must provide detailed information about the product, manufacturing process, ingredients, labeling, and safety data.
What is the purpose of food and drug administration?
The purpose of the FDA is to protect public health by ensuring the safety, efficacy, and security of food, drugs, medical devices, cosmetics, and other products.
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Information such as product description, manufacturing process, ingredients, labeling, safety data, and contact information must be reported on FDA forms.
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