Zdrowie i gospodarka · 10/05/2016

FDA Announces Draft Guidance for Premarket Tobacco Product Applications for Electronic Nicotine Delivery Systems

The Food and Drug Administration (FDA) has released a draft guidance to help manufacturers of electronic nicotine delivery systems (ENDS) prepare their premarket tobacco product applications (PMTA) in response to the agency's final rule deeming these products subject to the Federal Food, Drug, and Cosmetic Act (FD&C Act)