In requesting an easier path, the court wrote, the Industry impermissibly assumes the very public health conclusion that premarket authorization requires be substantiated before a product may be sold: that e-cigarettes are no more risky to the population as a whole than preexisting tobacco products, balancing the prospect that they may lead existing users to less harmful products or usage patterns against the risks that existing tobacco users will postpone reductions or intensify their usage and that non-users will start. [4] Thus, the fact that few e-cigarettes have been authorized does not suggest that the premarket review process as conducted by FDA has been flawed with respect to e-cigarettes or other claimed reduced risk products
Doctors call FDA authorization of e-cigarette sale, marketing alarming. ABC27, 20 October 2021, Accessed 20 December 2021
Airlines enforce a no-smoking, no-vaping policy inside the aircraft, regardless of the type of vaping device
Spain's main hospitality-sector lobby said in a statement it disagreed with the measure, which "would have very limited effectiveness, as it could drive smokers indoors to places such as private homes, thereby increasing exposure to second-hand smoke"