According to the requirements of the Amazon platform, the sale of cosmetics on the platform must comply with the corresponding export requirements of the countries to which they are destined. In the case of exporting cosmetics to the United States, for example, it is necessary to [...]
Toothpastes exported to the United States are regulated by the FDA, with specific requirements depending on whether they are classified as drugs or cosmetics. If the toothpaste claims to have anti-cavity or whitening effects or contains
Candy belongs to the FDA [Food] category, and the FDA requirements and procedures to be followed when exporting to the U.S. market are correct. The following are the regulatory requirements
Recently, many companies in the food industry have received important notices from the U.S. Food and Drug Administration (FDA) reminding them to update their information in the FDA system.
In the United States, although the Food and Drug Administration (FDA) does not require all products to be labeled with expiration dates across the board, expiration date labeling is regulated for certain products.
Under FDA regulations, food additives, as common and important ingredients in food, play a variety of roles, from enhancing aesthetics to maintaining food quality. Take
The U.S. Food and Drug Administration (FDA) and the U.S. Department of Agriculture (USDA) each have their own division of labor when it comes to food regulation. When categorizing and registering products, it is important for businesses to understand that the two organizations have different roles to play in food regulation.
🔍 Labeling in the food industry is an important link between consumers and manufacturers, and requirements for its accuracy are central to regulatory compliance. The following are FDA's requirements for food labeling
🌟 The Dun & Bradstreet (D-U-N-S® Number) has become a key identifier in the world of business, and this nine-digit code is not only
Green Circle Talks Cross Border] - FDA Registration: The Importance of DUNS Numbers Read More »
The U.S. Food and Drug Administration (FDA), as a scientific regulatory agency, is responsible for ensuring that food, cosmetics, drugs, medical devices, and other products manufactured or imported into the U.S. are safe and effective.
Cosmetic manufacturers and sellers are facing new compliance requirements as the U.S. Food and Drug Administration's (FDA) new regulations for the cosmetics industry take effect. Since 20
The recent passage of the Modernization of Cosmetic Regulation Act of 2022 (MoCRA Act) in the United States can be considered a revolutionary change that has made the entire cosmetics industry
The information FDA requires to be included on food labels is intended to protect the health and interests of consumers and to ensure that they can make informed decisions when purchasing and consuming food. The following
In this increasingly globalized business environment, credit and trust building is particularly important. You may be wondering how businesses can have any contact with each other without each other.
The FDA's risk assessment process for commodities is a complex system designed to protect public health and safety. The system evaluates products based on a number of key factors, including
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