What is the FDA?

FDA is the abbreviation of Food and Drug Administration, which is authorized by the U.S. federal government as the highest law enforcement agency specializing in food and drug administration, and is a governmental health control and monitoring agency comprised of doctors, lawyers, microbiologists, chemists, statisticians, and other professionals dedicated to protecting, promoting, and improving the nation's health. control and surveillance agency. Many other countries seek and receive help from the FDA to promote and monitor the safety of their products.

FDA's responsibility is to ensure that food, cosmetics, drugs, biologicals, devices, and radiological products manufactured in or imported into the United States are safe and effective for human consumption, and that FDA-approved food, cosmetics, and medical devices are safe and effective for human consumption. In nearly 100 countries, including the United States, only FDA-approved materials, devices and technologies can be commercialized for clinical applications.

What products require FDA certification?

According to the regulations, 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 must be inspected and certified as safe by the FDA before they can be sold on the market.

As the earliest consumer protection agency in the United States, FDA is responsible for the management and certification of all relevant food, drugs, cosmetics and radioactive devices in the U.S. FDA works closely with ISO and other international organizations, and is recognized by the World Health Organization as the highest food safety standard, and to this day, the FDA has become a global food and drug consumers in the heart of the Adamantine Shield.

Why do FDA certification?

As mentioned earlier, all U.S. domestic production or U.S. imports and sales of food, drugs, cosmetics, etc. must be certified by the FDA before entering the U.S. market sales. Because these products in the United States port of entry, will be carried out batch by batch of sampling, sampling samples qualified, the batch of products can be released, if unqualified, the FDA has the right to inspect the manufacturer, the right to prosecute offenders, but also can be carried out "automatic detention".

How to do FDA certification?

You know, FDA certification, can be said to be the highest honor and protection of the product, will be in the global market unimpeded. So how to do FDA certification?

1. Provide product information;

2. Evaluate the product information and make a quotation;

3. Sign a cooperation agreement and payment, fill out the application form;

4. Complete the registration and receive the FDA receipt.

PS: Chinese applicants in the FDA registration is required to assign a U.S. citizen (company / association) as its agent Oh, the laboratory has a branch in the United States, more professional engineers one-on-one service, the whole agent FDA certification services.