Hi: Thanks for the reply. The URL you listed - "http://....../rYTRUS" - is missing some info like domain name.
Hi: Thanks for the reply. The URL you listed - "http://....../rYTRUS" - is missing some info like domain name.
I certainly don't want my ability to vape or the industry hurt by regulation, but our other options weren't really great either. I feel like there are only a few ways this could have gone to maintain the industry's momentum.
New product status. If ecigs were stated as an entirely new product, like a personal electronic vaporizor etc... this would definitely require a large amount of studies and high costs in regards to the new product/technologies efficacy, social utility, potential harm to others and wouldn't allow people (like us) to be heard. Once the new product is submitted, the FDA would have had only 180 days to make a decision.
Substaintial Equivalency. If you are introducing a new tobacco product to the FDA as a new variant of a tobacco cigarette by blend, paper type or other change, you must submit an application and the FDA would have no set deadline for approval (they can review it indefinitely). I found the total number of product submissions received and filed each month, but can't find where any approvals are (help! if you can find them). The highest month (by a long shot to be fair) was March 2011 with the grand total of: 3,552 submissions.
So it seems to me that regulating this product as a tobacco product (that has a pretty long lineage behind it) was our best option if we wanted to keep up with the momentum the industry was going. What comes out from the FDA is a proposed rule, meaning they are going to publish a regulation (that doesn't have any force) open for review and comment prior to adoption. So because this is a tobacco product we get to have a voice, and I am personally happy for that. What we need to do is better prepare to respond to the proposed rule the most eloquently way possible. Which is why I wanted to start this thread, to see what people had to say about the topic and I'm really happy people are sharing their input!
Oh, so now it's a by-product!
I guess Coca-Cola is coffee then, because it contains caffeine.
And would tomatoes be tobacco products too?
50 people damaged by ecigs in the last year. Poison control center emergencies up. Nico poison complaints & shortness of breath etc. people are scared & the FDA to the rescue. Just heard on the radio 2 minutes a ago . Miami WIOD 610.
Now, what do you think is going to happen? Huh?..
Will there be some way to write them once the regulations are proposed for review? If so there are 13 vape shops here I will be going to to get them to write as well.I certainly don't want my ability to vape or the industry hurt by regulation, but our other options weren't really great either. I feel like there are only a few ways this could have gone to maintain the industry's momentum.
New product status. If ecigs were stated as an entirely new product, like a personal electronic vaporizor etc... this would definitely require a large amount of studies and high costs in regards to the new product/technologies efficacy, social utility, potential harm to others and wouldn't allow people (like us) to be heard. Once the new product is submitted, the FDA would have had only 180 days to make a decision.
Substaintial Equivalency. If you are introducing a new tobacco product to the FDA as a new variant of a tobacco cigarette by blend, paper type or other change, you must submit an application and the FDA would have no set deadline for approval (they can review it indefinitely). I found the total number of product submissions received and filed each month, but can't find where any approvals are (help! if you can find them). The highest month (by a long shot to be fair) was March 2011 with the grand total of: 3,552 submissions.
So it seems to me that regulating this product as a tobacco product (that has a pretty long lineage behind it) was our best option if we wanted to keep up with the momentum the industry was going. What comes out from the FDA is a proposed rule, meaning they are going to publish a regulation (that doesn't have any force) open for review and comment prior to adoption. So because this is a tobacco product we get to have a voice, and I am personally happy for that. What we need to do is better prepare to respond to the proposed rule the most eloquently way possible. Which is why I wanted to start this thread, to see what people had to say about the topic and I'm really happy people are sharing their input!
Will there be some way to write them once the regulations are proposed for review? If so there are 13 vape shops here I will be going to to get them to write as well.
Well that's bad. The FDA would have to change a few things to include e-cigs but it does look possible. I'm not sure they cold make the leap from nicotine base to tobacco so easily. I suppose synthetic nicotine would be a short circuit. I will have to ponder this. I think it would be absurd for such an action though.
This is probably old news to many but I think it won't hurt to re-quote it.
Quote from FDA -
"September 22, 2009 ... Family Smoking Prevention and Tobacco Control Act ...
According to the act
…a cigarette or any of its component parts (including the tobacco, filter, or paper) shall not contain, as a constituent (including a smoke constituent) or additive, an artificial or natural flavor (other than tobacco or menthol) or an herb or spice, including strawberry, grape, orange, clove, cinnamon, pineapple, vanilla, coconut, licorice, cocoa, chocolate, cherry, or coffee, that is a characterizing flavor of the tobacco product or tobacco smoke
Any company who continues to make, ship or sell such products may be subject to FDA enforcement actions."
The sad thing is there is so many people talking about banning, regulating, categorizing ecigarettes, yet there is not a single serious study based on real evidence about the side effects, consequences, or benefits of ecigarettes, all the politician's arguments backing their bills are BS, no solid evidence, we are guilty by association.
As a user of ecigs, I'd like to see a serious impartial, and scientific study about what vaping means for my health, not a stupid study done by this or that university with serious methodological and statistical deficiencies performed by a group of students who need to graduate or a group of so called scientists that need to come up with results in "something" in order to keep their funding.
So it seems to me that regulating this product as a tobacco product (that has a pretty long lineage behind it) was our best option if we wanted to keep up with the momentum the industry was going. What comes out from the FDA is a proposed rule, meaning they are going to publish a regulation (that doesn't have any force) open for review and comment prior to adoption. So because this is a tobacco product we get to have a voice, and I am personally happy for that. What we need to do is better prepare to respond to the proposed rule the most eloquently way possible. Which is why I wanted to start this thread, to see what people had to say about the topic and I'm really happy people are sharing their input!
You keep saying tobacco products. They already have most of this on tobacco products. You're talking about "nicotine" products, right? Or has e-juice already been officially classified as a "tobacco product". Please clarify.
I certainly don't want my ability to vape or the industry hurt by regulation, but our other options weren't really great either. I feel like there are only a few ways this could have gone to maintain the industry's momentum.
New product status. If ecigs were stated as an entirely new product, like a personal electronic vaporizor etc... this would definitely require a large amount of studies and high costs in regards to the new product/technologies efficacy, social utility, potential harm to others and wouldn't allow people (like us) to be heard. Once the new product is submitted, the FDA would have had only 180 days to make a decision.
Substaintial Equivalency. If you are introducing a new tobacco product to the FDA as a new variant of a tobacco cigarette by blend, paper type or other change, you must submit an application and the FDA would have no set deadline for approval (they can review it indefinitely). I found the total number of product submissions received and filed each month, but can't find where any approvals are (help! if you can find them). The highest month (by a long shot to be fair) was March 2011 with the grand total of: 3,552 submissions.
So it seems to me that regulating this product as a tobacco product (that has a pretty long lineage behind it) was our best option if we wanted to keep up with the momentum the industry was going. What comes out from the FDA is a proposed rule, meaning they are going to publish a regulation (that doesn't have any force) open for review and comment prior to adoption. So because this is a tobacco product we get to have a voice, and I am personally happy for that. What we need to do is better prepare to respond to the proposed rule the most eloquently way possible. Which is why I wanted to start this thread, to see what people had to say about the topic and I'm really happy people are sharing their input!