WEBINAR – E-Cigarette Regulation: The Past, Present, and Future of FDA’s Gatekeeping Role

According to federal law, all e-cigarettes must go through a process called “premarket review” in order to be commercially marketed in the US. So far, no e-cigarette has received marketing authorization from the FDA. Yet, after September 9th, 2021, the only e-cigarette products that should remain on store shelves are those that have received affirmative marketing authorization. This webinar will provide background of the premarket review process, update viewers on the progress of the FDA’s ongoing review process of millions of tobacco products, and discuss what might happen after the September 9th, 2021 deadline. 

REGISTER HERE