New tobacco products on the market without the required pre-market authorisation are marketed unlawfully and subject to enforcement action at the Food and Drug Administration (FDA)’s discretion.
All tobacco products that meet the definition of “tobacco product” in the Family Smoking Prevention and Tobacco Control Act – meaning nicotine pouches that derive from tobacco and synthetic nicotine – are subject to FDA enforcement actions.
This report analyses US federal enforcement actions in relation to nicotine pouches as well as examining the ten most populated states – including their localities – and their enforcement programmes.
Kristina holds a Masters Degree in International Law from Moscow State Linguistic University, Russia. In 2020 she completed a six-month exchange programme at the University of Malaga. She has worked as a legal secretary at the Ninth Arbitration Court of Appeal, Russia; and as a legal assistant in a law firm in Moscow.
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