Sounds like they are saying they are leaving the consumers who diy and build their own alone....for now...Appears I'm not the only one that stood out to.
Sounds like they are saying they are leaving the consumers who diy and build their own alone....for now...Appears I'm not the only one that stood out to.
I get what you're saying. So a quick rubber-stamping, if they can do that, would move the process along faster.
Excellent article here: When two tribes go to war
Didn't even think of the role reversal that England now plays in relation to US/World vaping rights. Kinda glad now that's the way things are. Wish it wasn't this way to begin with. But it does present another, highly prominent chance for resolution to the mess, and incorporates the scientific aspect.
Sounds like more than that to me. Almost like "For now we aren't going to enforce lack of a PMTA on anything but a complete ecig ready to vape" (cigalike)Sounds like they are saying they are leaving the consumers who diy and build their own alone....for now...
Hey, was doing some in depth late night reading. Digest this and tell me if you think this means what I think it might mean:
(Comment 26) Many comments stated that a requirement to prepare PMTAs for all of the many parts and components that go into some of the newly deemed tobacco products would create an effective ban of these products.
(Response) The definition of a tobacco product includes components and parts, and these products are subject to the automatic provisions of the FD&C Act, including premarket authorization requirements. However, at this time, FDA intends to limit enforcement of the premarket authorization provisions to finished tobacco products. In this context, a finished tobacco product refers to a tobacco product, including all components and parts, sealed in final packaging intended for consumer use (e.g., filters or filter tubes sold separately to consumers or as part of kits). For example, an e-liquid sealed in final packaging that is to be sold or distributed to a consumer for use in a finished tobacco product will be subject to enforcement if it is on the market without authorization. In contrast, an e-liquid that is sold or distributed for further
manufacturing into a finished ENDS product is not itself a finished tobacco product. At this time, FDA does not intend to enforce the premarket authorization requirements against such eliquids or other components and parts of newly deemed products that are sold or distributed solely for further manufacturing without a marketing order.
That's Marshal Zeller, now.
Sheriff, appointed to rope in the Wild West Industry and settle Vaping into the Dust once and for all. No good
It could become a hot issue in some State and local elections, and I'm hoping it will.Based on what I've seen and read, the general (ignorant) public is 100% behind the FDA action, so don't expect any candidate to go against it...
You're not the crazy one. FDA is.Am I crazy here?
There will prolly be a software update for my Evic VTC Mini upgrading it to 200 watts before August 8?
Based on what I've seen and read, the general (ignorant) public is 100% behind the FDA action, so don't expect any candidate to go against it...
A post 2 or 3 pages back, and another one somewhere, said the FDA doesn't charge fees, and the expenses are from preparing the application. I think that's correct.
Right, they probably are people who follow them because they are anti-Libertarian Party. I hope, anyway, 'cause, yeah, more than a bit disturbing, if they're Libertarians and have drunk the ANTZ Kool-Aid.I was quite dismayed earlier at something myself. The LP posted about it on FB and I glanced through the first hundred or so comments. Now remember that Libertarians should be almost in 100% (if not 100%) agreement with us. About 1 out of 15 of those comments were against ecigarettes and for the deeming and showed a total swollowing of media lies. Unless those comments against ecigs were by trolls who follow the LP's FB page I was flabbergasted.
Yes you are right. If ejuice vendors only sell the parts for everything needed but do not put them together then it is not an ENDS product( at least that is how it reads).Sounds like more than that to me. Almost like "For now we aren't going to enforce lack of a PMTA on anything but a complete ecig ready to vape" (cigalike)
Am I crazy here?
Course they could change that tomorrow if they so desire.
Edit: perhaps that is just to clarify whom has to have the PMTA?
Did you maybe think I said "processing the application" rather than "preparing" it? The expenses would be for testing (not by the FDA), and legal fees in writing up the application, etc.Seriously, 330,000 per ml / battery / per any single component for prep ?
El Chapo much ?
Based on what I've seen and read, the general (ignorant) public is 100% behind the FDA action, so don't expect any candidate to go against it...