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With approved packaging from the Food and Drug Administration, it means that the materials are safe to contain food products. You won’t have to wonder about the safety of your packaging materials, and neither will your customers.
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The FDA, or Food and Drug Administration, is a government agency operating under the United States Department of Health and Human Services (HHS). The FDA is primarily responsible for regulating medical products and tobacco, foods and veterinary medicine, and global regulatory operations and policy.
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The FDA Center for Drug Evaluation and Research (CDER) is the watchdog for potential medications seeking approval for use in the United States. For CDER to begin evaluating a drug, pharmaceutical companies must first do extensive testing and document the results. Those results are sent into the CDER, which assigns a team of doctors, chemists, pharmacologists, and other scientists to review the evidence.
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Guidance documents represent the agency's current thinking on a particular subject. These documents are prepared for FDA review staff and applicants/sponsors to provide guidelines to the processing, content, and evaluation/approval of applications and also to the design, production, manufacturing, and testing of regulated products.
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FDA approval of a drug means that CDER has reviewed data on the drug's effects, and the drug is determined to provide benefits that outweigh its known and potential risks for the intended population. The drug approval process takes place within a structured framework that includes:
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The federal register is one of the most important sources for information on what FDA -- or for that matter, what any government agency is doing. Published daily, Monday through Friday, the federal register carries all proposed and finalized regulations and many important legal notices issued by the various agencies, as well as presidential proclamations and executive orders.
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The FDA has particular requirements for the labels of the products it regulates. In particular, the FDA requires certain statements to be made on the Principal Display Panel (PDP) of many FDA-regulated products, such as the Net Quantity of Contents, Statement of Identity, etc. However, it is essential to note that the label requirements differ based on product classification. For example, while food labels must bear Nutrition Facts Panels, dietary supplements (although a subset of the food classification) are required to display Supplement Facts Panels.
We provide a range of FDA attorneys, FDA lawyers, and FDA consultant services to help businesses become FDA compliant. Contact us now at (305) 507-9843, or visit our website for more details about our FDA lawyer.
