US FDA official website Registration China Processing Center-Chinese solves the registration problem of US FDA official website for you.
● US Food and Drug Administration-FDA for short.
● FDA is an executive agency established by the US government in the Department of Health and Human Services (DHHS) and the Department of Public Health (PHS).
● FDA is recognized as one of the largest food and drug regulatory agencies in the world.
● The US FDA mainly controls and supervises products such as food, feed, medical devices, cosmetics and medicines entering the US market through registration.
The purpose and responsibility of FDA is to ensure the safety of food, cosmetics, medicines, biological agents, medical devices and other products sold in the American market.
● FDA registration in official website-also known as FDA anti-terrorism registration, its purpose is to collect information about enterprises and products entering the US market, so as to facilitate the prosecution of problems.
● FDA is responsible for issuing inspection regulations for food-grade materials. A third party with relevant laboratory qualifications can conduct relevant tests according to FDA regulations and issue an FDA inspection report.
● US FDA certification-The requirements for FDA certification of products currently exported to the US market are different according to categories, mainly including FDA testing and FDA registration.
● FDA registration in the United States is the FDA's registration requirement for enterprise and product information. Completing FDA registration and obtaining FDA registration certificate does not mean that the enterprise or product is recognized or recognized by FDA.
● Obtaining the FDA inspection report through FDA inspection can prove that the product meets the requirements of relevant FDA regulations involved in the inspection report.
Food and feed enterprises registered with FDA;
Ningbo Jietong Testing Co., Ltd. can provide efficient and professional FDA registration services for food and animal feed-related enterprises, so that you can easily get rid of all kinds of complicated FDA registration information. We can complete the official FDA registration of food and feed in the United States within 2 working days after the customer submits the application, and provide the FDA official website inquiry process and the FDA registration certification materials. The FDA registration number is 1 1, which will help your products export smoothly into the American market.
The FDA will also conduct spot checks on food and feed processing enterprises registered and shipped to the US market for a long time. At the same time, it can provide professional FDA factory inspection consulting services to help enterprises standardize production processes in advance, improve regulatory materials, and provide professional English translation throughout the factory inspection to solve the concerns of FDA factory inspection.
Food FDA registration classification:
1. alcoholic beverages. Infant food, including infant formula 3. Baked products 4. Beverage juice 5. Candy does not contain chocolate, specialty candy and chewing gum. Cereal products, breakfast food, instant/ready-to-eat cereals. Cheese and cheese products. Chocolate and cocoa products. Coffee and tea 10. Food pigment additive 1 1. Traditional food or meal replacement (including medical food) 12. Dietary supplement 13. Seasoning 14. Seafood products 15. Food additive 16. Food sweetener 17. Fruits and fruit products 18. Fruit or vegetable juice, pulp or refined products 19. Gelatin, curd, pudding mixture or pie stuffing 20. Ice cream and related products 2 1. Imitation dairy products. Macaroni or noodle products. Meat, meat products and poultry. Milk, butter or dried dairy products. Eat more dinner, gravy, sauces and special foods.
26. Nuts and edible seed products. Preparation of salad products. Eggs and egg products. Snacks 30. Spices, essences and salts. Soup. Soft drinks and water. Vegetables and vegetable products. Vegetable oil (including olive oil) 35. Plant protein products. Whole grains, rice products (flour) or starch 36.
Animal feed FDA registration classification:
1. cereal or cereal products. Oilseeds or oilseeds 3. Alfalfa products or Lespedeza products. Amino acids or related products. Animal products. Plants and herbs. Beer brewing products. Chemical preservative. Citrus products 10. Directly feed microorganisms 1 1. Distilled product 6543. 8+02. Enzyme 13. Fat or oil 14. Fermented products 15. Feed/forage 16. Human food by-products 17. Seafood 18. Dairy products 19. Mineral or mineral products. Mixed feed or special product 2 1. Molasses or syrup products. Nonprotein products. Peanut products. Processing animal waste. Residue 26 Professional additives 27. Vitamins or vitamin products. Yeast products. Mixed feed 30. Pet food 3 1. Pet snacks or chewing gum. Nutritional supplements for pets. Other unclassified products.
Medical devices, OTC drugs, laser products and cosmetics are registered in official website through FDA:
There are many kinds of products, including medical devices, over-the-counter drugs, laser products, cosmetics and so on. The relevant FDA registration in the United States has different requirements according to different types and product categories. We will eliminate all service processes and fancy introductions for disguised charges, and provide efficient solutions in time according to the latest regulatory requirements to minimize your expenses.
Food contact materials FDA testing (FDA food-grade testing) service.
The testing standards issued by FDA mainly include FDA testing of food contact materials and cosmetics. See the left column for FDA testing of cosmetics. The FDA's requirements for testing food contact materials are as follows:
1.FDA's test requirements for organic coatings, metals and electroplated products: American FDA CFR 2 1 175.300.
Deionized water leaching method for water extract
8% ethanol extract 8% ethanol leaching method
N-heptane extraction
2. FDA Testing/FDA Paper Products Testing Requirements FDA CFR 21176.170.
Pure chloroform soluble extract of chloroform soluble extract in water (deionized water leaching method)
Net chloroform soluble extract of chloroform soluble extract of 8% ethanol fraction (8% ethanol leaching method)
Net chloroform soluble extract of chloroform soluble extract of 50% ethanol fraction (50% ethanol leaching method)
Net chloroform soluble extract of chloroform soluble extract of n-heptane fraction (n-heptane leaching method)
3. FDA testing/FDA testing requirements for bamboo and wood products. FDA CFR 2 1 178.3800.
Pentachlorophenol and its salts
4.ABS/SAN FDA test /FDA test requires US FDA CFR 2 1 1 80.22 or 1 865 438+0.32.
Acrylonitrile residue in n-heptane or acrylonitrile residue in n-heptane
Residual acrylonitrile 8% ethanol in 8% ethanol
Residual acrylonitrile in 50% ethanol 50% ethanol
Acrylonitrile remaining in 3% acetic acid and 3% acetic acid
Acrylonitrile residue in acrylic acid residue in water
5.FDA test /FDA test requirements for acrylic acid) FDA resin FDA CFR 21177.1010.
Total extract (in water, 8%, 50% alcohol fraction, heptane) deionized water, 8%/50% ethanol and n-heptane.
KMnO4 oxidizable extract (in water, 8%, 50% alcohol fraction) Potassium permanganate can be oxidized and extracted.
Ultraviolet absorption (in water, 8%, 50% ethanol) Ultraviolet absorption (in water, 8% ethanol, 50% ethanol).
Ultraviolet absorption (in heptane) Ultraviolet absorption (in n-heptane)
6. Sealing rings and gaskets of food containers, such as silicone rubber rings, are FDA-tested /FDA-tested in the United States. FDA CFR 21177.1210.
Pure chloroform soluble extract of chloroform soluble extract in water (deionized water leaching method)
Net chloroform soluble extract of chloroform soluble extract of 8% ethanol fraction (8% ethanol leaching method)
Net chloroform soluble extract of chloroform soluble extract of n-heptane fraction (n-heptane leaching method)
7.EVA FDA testing /FDA testing requirements US FDA CFR 21177.1350.
Net chloroform soluble extract of chloroform soluble extract of water part
Net chloroform soluble extract of chloroform soluble extract extracted with 8% alcohol fraction and 8% ethanol.
Net chloroform soluble extract of chloroform soluble extract extracted with 50% alcohol fraction and 50% ethanol.
Chloroform soluble extract of n-heptane was extracted by pure chloroform soluble extract.
8. FDA testing requirements for melamine resin /FDA testing US FDA CFR 21177.1460.
Clean chloroform soluble water extract chloroform soluble extract (deionized water leaching method)
Clean chloroform soluble 8% ethanol extract chloroform soluble extract (8% ethanol leaching method)
Pure chloroform-soluble n-heptane extract chloroform-soluble extract (n-heptane leaching method
9. FDA testing of nylon plastics /FDA testing requirements FDA CFR 21177.1500.
Specific gravity density
Melting point
Solubility/boiling solubility of 4.2 n in hydrochloric acid
Deionized water leaching method for water extract
95% ethanol extraction
Ethyl acetate extraction method
Benzene leaching method of benzene extract
10. FDA inspection /FDA test requirements for PP plastics FDA CFR 21177.1520.
Specific gravity density
Melting point
N-hexane extraction method
Xylene leaching method of xylene extract
11.FDA inspection /FDA test requirements for PE plastics: FDA CFR 21177.438+0520.
Specific gravity density
N-hexane extraction method
Xylene leaching method of xylene extract
12. FDA inspection /FDA test requirements for perfluorocarbon resins. American FDA CFR 21177.1550.
Reflux extraction with 50% ethanol for 2 hours and reflux extraction with 50% ethanol for 2 hours.
N-heptane was extracted at reflux temperature for 2 hours, and n-heptane was refluxed for 2 hours.
Ethyl acetate was extracted at reflux temperature for 2 hours, and ethyl acetate was extracted at reflux for 2 hours.
Fluoride extract in distilled water (as fluoride)
Fluoride extract (calculated as fluoride) in 8% ethanol (used for coating) Fluoride extract (calculated as fluorine)
Fluoride extract in 50% ethanol (calculated as fluoride) 50% fluoride extract (calculated as fluoride)
Fluoride extract in ethyl acetate (calculated as fluoride)
Fluoride extract (based on fluoride) in n-heptane fluoride extraction (based on fluoride)
13. FDA inspection /FDA test requirements for PC plastics. American FDA CFR 21177.1580.
Water reflux extraction of water extract at reflux temperature
Reflux extracting with 50% ethanol at reflux temperature.
Reflux extraction of n-heptane at reflux temperature
14. FDA inspection /FDA test requirements for PET plastics FDA CFR 21177.1630.
Chloroform soluble fraction of distilled water: chloroform soluble extract extracted from the net value of chloroform soluble fraction of distilled water.
Chloroform soluble fraction of n-heptane extracted by net chloroform soluble fraction of n-heptane
Net chloroform-soluble fraction of chloroform-soluble extract extracted with 8% ethanol.
Net chloroform-soluble fraction of chloroform-soluble extract extracted with 50% ethanol.
Net chloroform-soluble fraction of chloroform-soluble extract extracted with 95% ethanol.
15.PS FDA test /FDA test requirements FDA CFR 21177.1640.
Residual styrene monomer residue
16.FDA inspection /FDA test requirements for polysulfone resin) FDA United States FDA CFR 21177 438+0655.
Deionized water leaching method for water extract
3% acetic acid extraction method
50% ethanol extraction method
N-heptane extraction n-heptane leaching method
17. Polyurethane resin