U.S. FDA

根據您提供的資訊以及《2022年化妝品法規現代化法案》（MoCRA）的規定，化妝品在FDA註冊中涉及的不良事件 […]

In the U.S., electric toothbrushes are categorized as medical device Class I products, and their market entry requires obtaining medical device FDA registration codes and meeting Federal Communications Commission (FC) requirements.

U.S. FDA Definition of a Laser Electronic Product The U.S. Food and Drug Administration (FDA) defines a laser electronic product as any product that contains an electronic circuit capable of emitting a laser light.

Under the FDA's latest regulatory update, efficacious cosmetics (OTC-Drugs), i.e., those products that function as both a cosmetic and a drug, must now be

Eye shadows and lip glosses, as cosmetic categories, must comply with U.S. Food and Drug Administration (FDA) regulations if they are intended for sale in the U.S. market. According to the latest

The U.S. Food and Drug Administration (FDA) is the government agency responsible for overseeing the safety of food, cosmetics, pharmaceuticals, medical devices, and radiated electronic products in the U.S. and abroad.

According to the requirements of the Amazon platform, the sale of cosmetics on the platform must comply with the corresponding export requirements of the country to which they are sold. In the case of exporting cosmetics to the United States, for example, it is necessary to

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

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.