From glantz blog
h ttps://tobacco.ucsf.edu/how-submit-public-comments-fda-ecig-and-cigar-deeming-and-ucsf-comments
Interesting to know, but this isn't to recommend or to not recommend doing the same.
Also glantz is reporting what a tobacco group (NATO) is telling their retailers regarding 'comments'
h ttps://tobacco.ucsf.edu/what-tobacco-retailers-are-being-told-say-fda-about-cigars-pipe-tobacco-and-ecigs
[Premarket Review Background: Do Not Include in Comments: For cigars, pipe tobacco, and electronic cigarettes, that were not on the market as of February 15, 2007, manufacturers of these products would need to submit a premarket tobacco application (PMTA) to the FDA within 24 months following the effective date of the final deeming regulations. If a PMTA application is filed with the FDA during this 24-month period, then the manufacturer can continue to market its products unless and until the FDA responds to the application. The standard to be used by the FDA in reviewing PTMAs will be whether the tobacco product is appropriate for the protection of the public health or detrimental to the public health.]
Also (just posted)
h ttps://tobacco.ucsf.edu/shareable-microsite-generate-comments-fda-deeming-docket
h ttps://tobacco.ucsf.edu/how-submit-public-comments-fda-ecig-and-cigar-deeming-and-ucsf-comments
Interesting to know, but this isn't to recommend or to not recommend doing the same.
Also glantz is reporting what a tobacco group (NATO) is telling their retailers regarding 'comments'
h ttps://tobacco.ucsf.edu/what-tobacco-retailers-are-being-told-say-fda-about-cigars-pipe-tobacco-and-ecigs
[Premarket Review Background: Do Not Include in Comments: For cigars, pipe tobacco, and electronic cigarettes, that were not on the market as of February 15, 2007, manufacturers of these products would need to submit a premarket tobacco application (PMTA) to the FDA within 24 months following the effective date of the final deeming regulations. If a PMTA application is filed with the FDA during this 24-month period, then the manufacturer can continue to market its products unless and until the FDA responds to the application. The standard to be used by the FDA in reviewing PTMAs will be whether the tobacco product is appropriate for the protection of the public health or detrimental to the public health.]
Also (just posted)
h ttps://tobacco.ucsf.edu/shareable-microsite-generate-comments-fda-deeming-docket
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