The U.S. Food and Drug Administration (FDA) examines, tests, and approves a wide range of items for medical use, including drugs, medical devices, food, cosmetics, and many other health-related products. In the simplest terms, "FDA approval" means that the FDA has decided the benefits of the approved item outweigh its potential risks. Now, new products must go through the FDA approval process before they are available to the public.
If you have any questions about FDA ingredient reviews or how an FDA regulatory attorney can help you, please feel free to contact Shehadeh Giannamore, PLLC at (305) 507-9843. You can also visit our website for more details.
Comments