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The new US federal legislation has brought synthetic nicotine products under the oversight of the US Food & Drug Administration (FDA), meaning all synthetic nicotine products have to go through a premarket tobacco product application (PMTA) process. This has led to several questions this report addresses, such as: what the new federal legislation means for synthetic nicotine products; what the concerns were that spurred this legislation; what the next steps will be for synthetic nicotine products; whether there any products that currently do not fit the definition, or whether all products will fall under FDA oversight, and a look into enforcement to see how the market is really going to play out.

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Berta Camps Bisbal

Senior legal analyst
Berta has a law degree from the University of Barcelona and a Juris Doctor degree from Nova Southeastern University (Florida). She has worked as a faculty assistant in legal research in Florida, was a member of the Law Review, and has interned for a magistrate judge of the US District Court for the Southern District of Florida. Berta focuses on US legal analysis, including tracking all federal, state and local regulation. She runs our US interactive regulatory tracker product, following changing regulation on e-cigarettes in all 50 US states.

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