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Dual route for E-cigarettes As proposed by MEPs, e-cigarettes would be regulated, either as medicinal products, if they are marketed as a quitting aid, or alternatively as tobacco products

Control 25 (5), 594604 (2016)

Table 1 Comparison of cigarette smoke exposed and non-exposed mothers and their infants

MANDO : Short for mandatory

The PMTA assessment process needs non-marginal re-engineering so that at least 4,000 ENDS products can be authorized (to compete against as many as 100,000 illicit products), that barriers to entry and application costs need to fall by a factor of at least ten (in line with the 2016 Deeming Rule Impact Analysis), and so that applications can be processed within 180 days (in line with the law)