The relationship between FDA and PMTA in the United States? Let's first understand what FDA and pmta are?

FDA is the abbreviation of the Food and Drug Administration. The FDA also sometimes represents the United States Food and Drug Administration. The FDA is authorized by the United States Congress, the federal government, and is the highest law enforcement agency specializing in food and drug management. It is also a government health control monitoring agency dedicated to protecting, promoting, and improving national health, composed of professionals such as doctors, lawyers, microbiologists, chemists, and statisticians.

The US FDA is one of the executive agencies established by the US government within the Department of Public Health (PHS) under the Department of Health and Human Services (DHHS). FDA mainly includes testing and registration. Medical devices, cosmetics, food and drug products require FDA registration. FDA registration can be directly applied for on the FDA official website.

PMTA, the full name of "Pre market Tobacco Application", refers to the pre market application for tobacco. According to regulations issued by FDA, electronic cigarette products are included in the scope of tobacco products and subject to FDA supervision. Products that have not passed PMTA certification are not allowed to be listed in the United States. As of September 9, 2020, the United States Food and Drug Administration requires all electronic cigarette products sold in the United States market to submit an ingredient list application.

Through the brief introduction of FDA and PMTA, we understand that FDA is the Food and Drug Administration of the United States, and PMTA is a certification applied for by the PDA before tobacco is marketed.