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If scientific evidence indicates that the net gains of these products no longer outweigh the risks at the population levelor if the company fails to conduct the required postmarket surveillance and studiesthe FDA is committed to taking action as appropriate, including withdrawing the order, to protect public health. The modified risk tobacco product process outlined in the 2009 Family Smoking Prevention and Tobacco Control Act allows companies to submit applications for the FDA to evaluate whether a tobacco product may be sold or distributed for use to reduce harm or the risk of tobacco-related disease

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J Public Health (Berl.) 33 , 11351144 (2025)