Boutique Articles

罐裝食品工藝指的是將食品加工後密封在容器內，如罐頭、瓶子、半硬包裝或軟包裝等。由於過去因為熱處理不足或酸化處理 […]

The FDA's definition of cosmetics does include a range of products that are used in various forms in everyday life for the purpose of cleansing, beautifying, increasing attractiveness, or altering the external

Based on the information you have provided and the provisions of the Modernization of Cosmetic Regulations Act of 2022 (MoCRA), adverse events involved in FDA registration of cosmetic products

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.