Certifications

USFDA REGISTRATION

UNITED STATES FOOD AND DRUG ADMINISTRATION AGENCY REGISTRATION

The United States Food and Drug Administration (FDA) is a Federal Agency of the Department of Health and Human Services. The FDA is responsible for Protecting and Promoting Public Health through the Control and Supervision of Food Safety, Tobacco Products, Dietary Supplements, Prescription & Over-The-Counter Pharmaceutical Drugs (Medications), Vaccines, Biopharmaceuticals, Blood Transfusions, Medical Devices, Electromagnetic Radiation Emitting Devices (ERED), Cosmetics, Animal Foods & Feed and Veterinary Products. In order to be able to sell a product in the United States, you need to register with the US Food and Drug Administration for US FDA Registration. This is a process that involves submitting an application and paying a fee. Every company that makes a product for sale in the USA is required by law to register with the FDA. This assures that all items sold in the United States meet a set of quality criteria. FDA Registration benefits both consumers and companies. Those registered with the FDA are eligible for a variety of marketing advantages that might help them boost their overall business and exports to USA as well as other countries. The FDA regulates many products that are intended for human consumption, including food and medical devices. In addition to registering your product with them, you will also need to comply with all other applicable laws and regulations. This includes following Good Manufacturing Practices, which are guidelines for how to manufacture products safely. When you register your product with the FDA, you’re confirming that it’s been tested and found to be safe for public use. You also have to include information about how to use the product, what results you can expect from using it, and any possible side effects or risks.