What is the FDA? U.S. Food and Drug Administration (English full name: Food and Drug Administration, referred to as: FDA), FDA is the U.S. government in the Department of Health and Human Services (DHHS) and the Department of Public **** Health (PHS) in the establishment of one of the executive agencies. As a scientific regulatory agency, FDA is responsible for ensuring the safety of food, cosmetics, drugs, biologicals, medical devices, and radiological products manufactured in or imported into the United States. It was one of the first federal agencies whose primary function was to protect consumers. The agency is relevant to the lives of every U.S. citizen; internationally, the FDA is recognized as one of the largest food and drug regulatory agencies in the world; and many other countries seek and receive help from the FDA to promote and monitor the safety of their products.
Chinese name: FDA certification. Nationality:United States . FDA Certification. Certification program: food, agricultural products, seafood and so on. Alias Food and Drug Administration.
FDA Certification. Type of scientific management organization. Main testing items: food freshness, food additives and so on.
The agency is relevant to the lives of every U.S. citizen. Internationally, the FDA is recognized as one of the largest food and drug regulatory agencies in the world. Many other countries promote and monitor the safety of their country's products by seeking and receiving help from the FDA.
The Food and Drug Administration (FDA) is responsible for supervising and inspecting: food, drugs (including veterinary drugs), medical devices, food additives, cosmetics, animal food and drugs, wine beverages with an alcohol content of less than 7%, and electronic products; it also includes cosmetics, products that emit radiation, and combination products, such as electronic products and medical products, that are related to personal health and safety. Products in the use or consumption process of ionic, non-ionic radiation affecting human health and safety project testing, inspection and certification. According to the regulations, the above products must be tested and certified as safe by the FDA before they can be sold in the market. the FDA has the right to inspect the manufacturers and the right to prosecute the violators. According to the supervision of different product range, can be divided into the following major regulatory agencies:
1, the Center for Food Safety and Practical Nutrition (CFSAN):
The center is the FDA's largest workload department. It is responsible for food safety throughout the United States, except for meat, poultry and eggs, which are under the jurisdiction of the U.S. Department of Agriculture. Although the United States has one of the safest food supplies in the world, approximately 76 million foodborne illnesses occur each year, 325,000 people require hospitalization for foodborne illnesses, and about 5,000 people die from foodborne illnesses. The Center for Food Safety and Nutrition works to reduce foodborne illness and promote food safety. It also promotes a variety of programs, such as the promotion of HACCP programs.
The functions of the Center include: ensuring the safety of substances and colors added to foods; ensuring the safety of foods and ingredients developed through bioprocesses; being responsible for regulatory activities in the proper labeling of foods (e.g., ingredients, nutritional health claims) and cosmetics; developing appropriate policies and regulations for the management of dietary supplements, infant food formulas, and medical foods; ensuring that cosmetic ingredients and products are safety and ensure proper labeling; monitoring and regulating post-sale practices in the food industry; consumer education and behavioral outreach; cooperative programs with state and local governments; and coordination of international food standards and safety.
2. Center for Drug Evaluation and Research (CDER):
The Center is designed to ensure the safety and effectiveness of prescription and over-the-counter drugs, evaluates new drugs before they are introduced to the market, and monitors more than 10,000 drugs on the market to ensure that the products meet the highest standards of continual updating. The Center also regulates the truthfulness of advertisements for medicines on television and radio, as well as in publications. It strictly monitors medicines to provide consumers with accurate and safe information.
3. Center for Device Safety and Radiation Health (CDRH):
The Center ensures the safety and effectiveness of newly released medical devices. That's because there are more than 20,000 companies around the world that produce more than 80,000 different types of medical devices, from blood glucose monitors to artificial heart valves. Since these products are closely related to human life, the Center also oversees nationwide after-sales service. The center also sets safety standards for products that produce radiation, such as microwave ovens, televisions and cellular phones.
4. Center for Biologics Evaluation and Research (CBER):
This center regulates biological products that can prevent and treat diseases, and is therefore more complex than chemically synthesized medicines, and includes scientific research on the safety and efficacy of blood, plasma, and vaccines.
5. Center for Veterinary Medicine (CVM):
FDA Encyclopedia entry/v2394994.htm
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