1. Introduction to FDA certification

The Food and Drug Administration (FDA) is one of the executive agencies established by the US government in the Department of Health and Human Services (DHHS) and the Department of Public Health (PHS). As a scientific regulatory agency, FDA's role is to ensure the safety of food, cosmetics, pharmaceuticals, biologics, medical devices, and radioactive products produced or imported in the United States. It was one of the first federal agencies to protect consumers as its primary function.

Strictly speaking, there is no FDA-certified name, which the FDA itself said; but generally speaking, the FDA certification mainly refers to the following two types:
     1. FDA registration: Many products are sold to the United States for registration (such as food, medicine, medical equipment, laser products, etc.), and some products must be tested before they can apply for registration;
     2, FDA testing: is to test the product in accordance with FDA regulations;
    The Food and Drug Administration (FDA) is one of the executive agencies established by the US government in the Department of Health and Human Services (DHHS) and the Department of Public Health (PHS). As a scientific regulatory agency, FDA's role is to ensure the safety of food, cosmetics, pharmaceuticals, biologics, medical devices, and radioactive products produced or imported in the United States. It was one of the first federal agencies to protect consumers as its primary function.

二．FDA certification

　　Most products FDA registration does not require fees, such as cosmetics, food, etc. These are not required to pay fees, only medical equipment products need to pay the US FDA fees, the other is the need for service fees. These testing certifications have produced many FDA-certified tests, one of which is the professional treatment of FDA testing of various products, FDA registration matters.

三．US FDA certification test

　　1. Various FDA tests for food contact materials, packaging materials, etc.;
       2. Food FDA factory registration;
       3. Cosmetics FDA factory registration or recipe registration;
       4. FDA registration of a class of medical device products, UDI application, D&B code application, etc.;
       5. Laser product FDA registration;

　  四.FDA-certified process

　　1. Distinguish the product, suitable for the test specification referral test project, suitable for the registration of the registration specification for registration;
      2. Fill in the test or register the relevant application form;
      3. Need to provide sufficient samples to the laboratory for testing;
      4. Both parties sign a quotation contract to arrange payment;
      5. Issue a qualified report or register a certificate after passing the test.

　　五.What are the benefits of the product passing the US FDA certification?

　　Ion, non-ionic radiation generated during the use or consumption of products affects the testing, testing and certification of human health and safety programs. According to regulations, products must be FDA-approved for safety before they can be sold in the market. The FDA has the right to inspect the manufacturer and have the right to sue the offender. According to the different product scope of supervision.

　　六.The role of FDA certification:

　　The FDA has a profound influence in the United States and the world, and is known as the "American health patron". The declared products need to be monitored by 143 key inspection points after the human body uses the products, and the products that have passed the monitoring of 2-3 million for 3-7 years, all of which pass the certification, will be issued FDA certification. Therefore, FDA certification is recognized by the World Health Organization as the highest food safety standard. It is the highest honor and guarantee pursued by international manufacturers.
       The FDA International Free Sales License is not only the highest level of certification in the US FDA certification, but also the highest pass certification for food and medicine approved by the World Trade Organization (WTO). It is the only one that must be fully approved by the US FDA and the World Trade Organization. Certificate of certification. Once this certification is obtained, the products will be open to any WTO member countries, and even the marketing model, the host government should not intervene.
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