Moreover, the proposed regulations do nothing to directly regulate product safety. For years to come, we would still have exploding batteries, leaking cartridges, and packaging that is not child-proof. After all, it is going to be a minimum of one year before the regulations are promulgated, another two years before the applications are due, and probably 5-6 years before the 22,000 new product applications can be processed (and that is only if the FDA acts in an unprecendentedly speedy fashion). So we're talking 8-9 years before we see any meaningful safety improvements.

Another recent study published late May in the Addiction Journal showed that the e-vapor produced in electronic cigarettes “can contain some of the toxinspresent in tobacco smoke, but at levels which are much lower.” This study conducted by 5 researchers, 2 of which were linked to a Federal Drug Administration tobacco panel, used approximately 81 different studies during its overall review. In conjunction, a scientific review on e-cigs from theconcluded with the comparison of conventional cigarettes, claiming that they are less likely to be as harmful. Peter Hajek of Londons Queen Mary University states “the evidence we currently have is clear: e-cigarettes should be allowed to compete against conventional cigarettes in the marketplace. Health care professionals may advise smokers who are unwilling to cease nicotine use to switch to e-cigarettes. Smokers who have not managed to stop with current treatments may also benefit from switching to e-cigarettes.”

Moreover, several former members (and one current member) of the FDA's Tobacco Products Scientific Advisory Committee have (or have had) financial conflicts of interest with Big Pharma, and thus are not in a position to offer opinions about national tobacco product regulation in the context of this expert advisory panel.

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