AEMSA FDA Public Comment Submission (FDA Docket No.: FDA-2013-N-0227)

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December 22, 2017

Via Electronic Submission (

Division of Dockets Management (HFA-305) Food and Drug Administration
5630 Fishers Lane, RM. 1061
Rockville, Maryland 20852

Re: Request for Comments for Industry Proposal for “Tobacco Product Manufacturing Practices for Electronic Nicotine Delivery Systems”; FDA Docket No.: FDA-2013-N-0227

The American E-Liquid Manufacturing Standards Association (AEMSA) appreciates this opportunity to respond to the Food and Drug Administration (FDA or Agency) request for comments on the updated recommendations for regulations on Tobacco Product Manufacturing Practices (TPMPs) for Electronic Nicotine Delivery Systems (ENDS) that were submitted to FDA by a group of industry stakeholders (FDA Docket No. FDA-2013-N-0227). This comment provides background on AEMSA’s voluntary standards and feedback on the proposed TPMPs. As described herein, AEMSA supports responsible, science-based and appropriate tailored regulations for ENDS, including good manufacturing practices…

To read the full comment submission, please download the PDF available here:
AEMSA TPMP Comment – FDA-2013-N-0227