The U.S. Food and Drug Administration is abbreviated as FDA, which governs products such as foods, drugs, medical devices, cosmetics, and radiation-emitting electronic products, etc. The FDA adopts post-market regulation for all companies, which means that a company can first make an FDA registration, export. During the export process, the FDA will regulate compliance through customs sampling, factory inspections, foreign supplier verification programs, and other measures.
The U.S. Food and Drug Administration (Food and Drug Administration) is referred to as the FDA, which is one of the executive agencies of the U.S. government established in the Department of Health and Human Services (DHHS) and the Department of Public **** Health (PHS). As a scientific regulatory agency, FDA's responsibility is to ensure the safety of food, cosmetics, drugs, biologicals, medical devices, and radiological products manufactured in or imported into the United States, including products that emit radiation, combination products, and other electronic and medical products that are related to personal health and safety. It was one of the first federal agencies to have consumer protection as its primary function.
@Registrar Corp provides FDA regulatory assistance to companies in the following industries:
- Food and Beverage
- Medical Devices
- Pharmaceuticals
- Cosmetics
- Other Industries
For more information on FDA registration/certification, please contact us at #Registrar Corp. You can contact us at #Registrar Corp#