Is is okay for a foreign (or American) company to sell or market a new drug and drug delivery
device to the American consumer without that product having met specific safeguards, all carefully spelled out in law and met by other products of a similar ilk?
Wait a second here. Thousands upon thousands of drugs are marketed every day in the USA. These drugs have the appropriate disclaimer attached to them, which is "These statements have not been evaluated by the FDA...etc etc etc".
So, where would e-smoking be different than say, chromium supplements or Vitamin E marketing materials?
What about some prescription drugs which have the same disclaimers?
Where do you really draw the line? Do you force every company to put everything through extensive testing, only for that test to yield a different result in the southern hemisphere, therefore disproving scientific duplication of results?
Now, there are many people who would say "WE MUST BE SAFE!" but be careful who you give that power to. You'll end up making an industry where only the richest companies can even think about bringing product to market...meaning the first companies to pass will be the only companies around in 30 years.
There is extreme *waste* in your proposal. Extreme wastes that will make candy bars become $20.00 in price due to extremely high development costs.
There's a certain degree of this already in this country. A new company trying to cut into big company profits (can we say "Delorean", forgot how to spell it) will get snuffed out even though their design is extremely good and ahead of it's time.
We really need to think of such statements...
Now, I would have a different opinion if, say, we heard news reports that 300 people died while using e-cigs and there is extreme concern with results that show some actual harm. But we're not seeing that, are we? We're not seeing people dying and croaking from using e-cigs. Jumping the gun and throwing extreme regulation into the mix before any results, good or bad, are published is just as damaging as no regulation at all. Actually, it's more damaging because it already sets precedent that the device is bad.
Think of this the next time you buy your Vitamin E supplement that has 500% of the USDA recommended daily allowance...because you're "trying to make your eyes better".
I would be very careful to call for regulation on e-cigs until the evidence is damaging or supporting. Until then, it is only fear, uncertainty, and doubt. Throwing regulation before product goes to market will make this depression even greater...because only the very large companies will prevail.
And let's not forget something...a "drug" is "a substance that is used as a medicine or narcotic"
So..
Medicine: (medicine) something that treats or prevents or alleviates the symptoms of disease
Narcotic: a drug that produces numbness or stupor; often taken for pleasure or to reduce pain; extensive use can lead to addiction
Numbness: partial or total lack of sensation in a part of the body; a symptom of nerve damage or dysfunction
Stupor: grogginess: marginal consciousness
Now, you look at those definitions. Tell me how it fits into e-cigs. Now think about how it fits into e-cigs when Nicotine is not part of the equation.
Why would you regulate it?