So how do ANTZ' plans for mandating lowering nicotine content in cigarettes jive with this, especially considering the disasterous health consequences of past promotion of low tar and nicotine cigs? Do they think that the resulting increase in intake of smoke by smokers to get their desired/needed nicotine will be safer, since the new plan will deliver more tar when only lowering the nicotine and not the tar? And how does it "not raise different questions of public health when compared to" the predicate products?The agency concluded that the products have different characteristics than the predicate products and Reynolds failed to show that the new products do not raise different questions of public health when compared to them.
I don't remember ever hearing about Preston Tucker before. After seeing your post, I read the Wikipedia article on him. Amazing story! There are some disturbing parallels to FDA and vaping.Sure glad that nothing like this has ever happened before in the US ...
Unless you count that business with Preston Tucker ...![]()
Substantial Equivalence has been discussed here many times over the years.
--There are those that understand
--There are those that close their eyes and hope it's all a bad dream
--There are those that deny that this will happen to electronic cigarettes
But yes, this is exactly how the electronic cigarette market can be destroyed.
Oh, no... They are using the 2007 date? Eww....
That grandfather date was in the original Family Smoking Prevention and Tobacco Control Act, and has been used against earlier 'new products' in cigarettes and cigars. The 'deeming' is only a 'proposed rule' which would of course use the same date as written.
E-liquid was around in 2007, was in not?
Why on earth would they insist on using the same 2007 date, retroactively, for e-cigs.
E-cigarettes were originally developed and patented in 2003
by Ruyan Group (Holdings) Ltd., a company based in Beijing.
Since their introduction into the U.S. market around 2006–
2007....
http://www.khlaw.com/webfiles/What_To_Expect.pdf
If the FDA imposed this
same Feb. 15, 2007, grandfather date to e-cigarettes, which,
strictly speaking, it is required to do, e-cigarette companies
would be required to submit premarket applications to the
FDA for all of their products sold after the grandfather date—
which would be practically all of the products currently on
the market .Such a rule would immediately disrupt the U.S.
e-cigarette industry and could result in such products being
pulled off the market. We believe this is highly unlikely, how
-ever, for several reasons.
The author is not only opposed to the 2007 date, he either thinks it's unlikely they'll got through with it, or that somehow they'll do it in a way that won't disrupt the market as much. I not sure how he means the part in bold of the following:
Yeah, I read it, but still not clear.Well.... the rest of the article explains the 'several reasons' see a, b, c, etc. after that comment.
I believe that putting up major roadblocks to e-liquid has been a big part of their plan.Nic, we don't really know what the FDA will do--there are many different analyses (tea leaf readings) from different experts, you can just Google it if you want to read more. Here's one from Bill G.
What is the Grandfather Date of the Tobacco Control Act & How Will it Impact the Vapor Industry? - SFATA | Smoke Free Alternatives Trade Association
"Even worse for vapor product industry is that FDA’s proposed deeming regulation would effectively ban the sale of all bottles of nicotine containing e-liquid because FDA would require manufacturers to submit studies and lab tests of each e-liquid product when used with each of the hundreds (or thousands) of different premium vaporizers, or open tank systems on the market."
He's basically saying that they have no choice but to do it, but he doesn't believe they will.Yeah, I read it, but still not clear.
Yeah, I read it, but still not clear.