We provide a range of FDA attorney, FDA lawyer and FDA consultant services to help businesses become FDA compliant. We serve a global clientele in any location.
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.
We provide regulatory guidance and FDA compliance services to a wide variety of clients who need assistance with establishing and maintaining full compliance with federal laws and regulations. Call us today at (305) 507-9843 or visit us online for more details.
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.
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Because the FDA generally classifies the products it regulates based on intended use and ingredients found therein, among other considerations, an initial stage in determining how a product will be regulated is by looking to the intended use. The FDA generally determines the intended use of a product based on statements, called “claims,” made about a product, i.e., what the marketer claims the product can do. By understanding the types of claims under FDA regulations and federal law, we can help you avoid making disease claims that may cause your products to be regulated as drugs inadvertently.
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While there are different types of claims, i.e., health claims, disease claims, structure-function claims, some claims may cause a product to be subject to heightened regulation. For example, if a product is otherwise classified as food, but its labeling contains disease claims, the FDA will classify this product as a drug. On the other hand, certain claims, called structure-function claims, may be made about dietary supplement products and, if done correctly, will not cause these products to be subject to heightened regulation.
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When a drug or treatment enters the clinical trial process, it must pass through three phases of testing before becoming eligible for the Food and Drug Administration (FDA) approval. Only if the treatment proves to be safe and promising at each phase, is it allowed to proceed to the next phase of testing.
If you need help with labeling and registering and listing your products with the FDA, you're in the right place! Call Shehadeh Giannamore, PLLC now at (305) 507-9843 for the best FDA attorney services, or you can also visit our website for more details.
FDA label reviews and marketing reviews are key tools that we use to help our clients comply with FDA regulations and related federal laws. Since the FDA generally classifies the products it regulates based on the intended use and ingredients found therein, an initial stage in determining how a product is regulated is by looking to the intended use thereof.
If you still need questions with FDA label reviews and FDA regulations, we've got you covered. Shehadeh Giannamore, PLLC, can assist you with establishing the best FDA compliance services! Give us a call now at (305) 507-9843, or you can also visit our website for more details.
While warning letters are considered an informal mechanism of agency action, the failure to respond appropriately may often result in more formal measures being taken against non-compliant firms. Because appropriate corrective measures often preclude further enforcement, it is critical to be vigilant when preparing FDA a warning letter response to perceived deficiencies in compliance. Accordingly, an FDA regulatory lawyer can allow you to develop a warning letter response that can help you avoid further agency enforcement.
For more information about hiring an FDA regulatory lawyer to help you respond to FDA warning letters or how you can achieve FDA compliance, please feel free to contact us now at (305) 507-9843. You can also visit our website for more details about our FDA attorney services.
