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This paper will evaluate the Master Settlement Agreement from a historical perspective, neoclassical approach, and an institutional approach

"While a new tobacco product can be legally sold if FDA authorizes it through the premarket tobacco product application (PMTA) pathway, seeking FDA authorization of the product through the optional MRTP pathway presents a meaningful harm reduction opportunity for manufacturers to communicate that certain products present a lower risk of tobacco-related disease, providing adults who smoke with the ability to make more informed decisions," the agency wrote in a Tuesday news release

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