Panel Discussion & Q&A: Will a regulated environment improve the dialogue on harm reduction
Time: 2:45 pm - 3:15 pm
Date: May 17 2022
may-17-2022 14:45
may-17-2022 15:15
Europe/London
Panel Discussion & Q&A: Will a regulated environment improve the dialogue on harm reduction
Has the lack of federal regulation led to a “wild west” for lawmakers and industry? “Big Tobacco” v Vape Stores –what are the regulatory implications for both, what significance will this have Will there be enough PMTA approved products to meet adult demand? Will the PMTA process create a 2-tier product category and a black… Read more »
The E-Cigarette Summit USA- Has the lack of federal regulation led to a “wild west” for lawmakers and industry?
- “Big Tobacco” v Vape Stores –what are the regulatory implications for both, what significance will this have
- Will there be enough PMTA approved products to meet adult demand?
- Will the PMTA process create a 2-tier product category and a black market?
- Do people working in public health, Research and tobacco control know enough people who smoke?
Chair
Prof David L. Ashley Ph.D RADM (retired) US Public Health Service: Research Professor - School of Public Health - Georgia State University
Speakers
Matthew R. Holman Director, Office of Science (OS),Center for Tobacco Products (CTP) - U.S. Food and Drug Administration
David Graham Chief Impact Officer - NJOY
Marc Slis Vape Shop Owner - Vaper & Former Smoker - Onboard Seismic QC
Prof Kathleen. S Hoke, J.D. Director of the Legal Resource Center for Public Health Policy - University of Maryland Carey School of Law
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