What I took away was this:
1-We don't know if e-cigs are safe, because we don't have a conclusive study.
2-If they are safe and do work, they should be classified as drug delivery devices, not tobacco products.
3-We don't know if e-cigs are safe, because we don't have a conclusive study.
They're basically saying they don't want any blood on their hands if something turns out to be bad about e-cigs in the long term, and if it turns out they ARE okay, then they should be used as a step-down device, I'm assuming under a doctor's supervision, with the end result being quitting both smoking and the e-cig.
I'm sure this has been talked to death, but what sort of study by what sort of organization would satisfy the nay-sayers? It seems as though one or two good thorough studies could put the whole thing to bed, so how do we as a group get that done? It seems like that should be the number one priority of every pro-vape group that exists (including consumers, retailers, and manufacturers).
And another question - I always see it referred to as a choice between two options, either drug delivery (cessation aid) or tobacco product. Shouldn't there be a third class, specifically for harm reduction products? Why can't we push for re-classification into a new category? It would give some legitimacy to these products, and address the very real shortcomings of both smoking and traditional NRTs.
It's ultimately a question of health - what actions would best protect public health? If NRT products have been "proven" effective - even with their abysmal track record for long-term success - it should be relatively easy to prove that not only do e-cigs pose very little threat, but they also have a remarkably high success rate.