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This document discusses how Intellareturn proposes to enhance the medical device return supply chain through the use of RFID technology for tracking warranties and defective products under the FDA's
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FDA can empower by providing regulations and guidelines to ensure the safety and efficacy of drugs, medical devices, and food products.
Manufacturers, importers, and distributors of drugs, medical devices, and food products are required to file with the FDA to comply with regulations.
To fill out FDA forms, applicants must provide accurate information about their products, including ingredients, manufacturing processes, labeling, and intended use.
The purpose of FDA empowerment is to protect public health by ensuring the safety, effectiveness, and quality of drugs, medical devices, and food products.
The information reported to FDA includes product formulation, manufacturing facilities, labeling, adverse events, clinical trial results, and any changes made to the product.
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