ntroduction of the FDA certification (Us food and drug Administration)
 

Food and Drug Administration in the United States (Food and Drug Admistraton abbreviation as FDA), belonging to the health education and Welfare Department, responsible for the national drug, food, biological products, cosmetics, veterinary drugs, medical equipment and supplies management diagnosis. FDA consists of the pharmaceutical Bureau, Food Bureau, veterinary drug administration, Radiological Health Bureau, Biological Products Bureau, medical instruments and diagnostic supplies Bureau, and National Toxicology Research Center, regional work management organization, that is, the 6 bureaus (some publications, also called 6 centres), a center and a regional management organization. The United States Food and drug administration has about 7500 staff members and 1143 FDA headquarters, of which 350 are from the drug administration. The United States Food and drug administration has about 7500 staff members and 1143 FDA headquarters, and of which 350 are from the drug administration.
 
Drug Administration (also known as drug evaluation and Research Center) responsible for the drug approval, there are 8 offices and a number of departments.
1.         Drug administration: It has 4 departments, such as drug information, information system design, administrative management and budget, and medical libraries.
2.         Office of drug control: There are 7 departments, such as drug quality evaluation, drug label supervision, production and product quality, scientific research, regulations and so on.
3.         Drug standards division: There are 2 sections including common drug evaluation, drug listing and advertising.
4.         Drug first review division: There are 5 departments including cardiovascular, kidney, antineoplastic agents, nutritional, medical, contrast and dental, gastrointestinal, and blood clotting drugs.
5.         Drug second review division: There are 3 sections including the anti infective drugs, metabolic and endocrine drugs, antiviral drugs.
6.         Department of epidemiology and biostatistics: There are 2 departments for epidemiology and investigation and biostatistics.
7.         Research office: It consists of 2 department, research and test, and drug analysis.
8.         Generic drugs division: There are 2 departments of generic drugs and biological equivalent.
 
 
The food and drug administration is based in Washington, D. C., and Marley, Lanzhou; it has a large body and branches throughout the country. In order to strengthen the quality control of drugs, FDA divides the whole country into 6 big areas, including Pacific area (San Francisco, Seattle, Los Angeles), Southwest (Dallas, Denver, Kansas), central and western regions (Chicago, Minneapolis, Detroit), The northeast region (Boston, New York, Buffalo), in the District of the Atlantic (Philadelphia, Cincinnati, Newark, Baltimore), The southeastern region (Atlanta, Nashville, New Orleans, Orlando, Victoria, Saint Ji'an). A large area is set up in each district, and a number of districts are set up in the large area. the Pacific region is located in San Francisco, the southwestern region is located in Dallas, the Central and Western Regions is located in San Francisco, the northeast is located in Boston, the large area of central the Atlantic is located in Philadelphia, and the area of the southeast is located in Atlanta.
 
District is responsible for the region's food, drugs, cosmetics, equipment, blood banks and other supervision and inspection work. A number of workstations are set up in each region as required, to ensure that the work area can cover the scope of the area. There are now 143 workstations in the United States. The big districts, districts and workstations are all directly affiliated institutions at FDA. The size of the district depends on the amount of work done; more than 65% of medicines in the United States are produced in central the Atlantic, so the area is stronger, there are total of 525 workers, including supervisors 250, which accounting for about 1/4 FDA headquarters supervisor, the analysis and inspection personnel are 150.
 
The management of drugs in each States is governed by local drug control regulations, the main task is: examination and registration of pharmacists, to supervise and inspect the drug administration departments and pharmacies, issue or renew a permit, revoke the license of the illegal household, evaluate the pharmacy schools where they are located, review the trainee pharmacy etc..
 
Note: FDA is a law enforcement agency, rather than services. If someone says they are under the FDA certification laboratory, then at least he is misleading to consumers, because FDA is neither affiliated the service certification authority and the laboratory with the public, nor the designated laboratory. FDA as a federal law enforcement agency, cannot do the referee, and do the athlete again. The FDA will only authenticate the GMP quality of the service laboratory, when it pass, just issue the certificate. But not "Specify" to the public, or recommend specific one or several, because which is against the principle of fair competition in American society.