by Alexandra Noel, Matthew Campen, and Willie McKinney, Ph.D. E-cigarettes are new but rapidly evolving class of products on the […] Read More
6 min. read
Resources
2 min. read
Perceptions and Use of an ENDS Device for a Vulnerable Population: Incarcerated Persons
Poster presented at TSRC 2022 by Cheryl K. Olson, M.P.H., Sc.D, Neil Sherwood, Ph.D, and Willie McKinney, Ph.D. Smoking in […] Read More
1 min. read
Market survey of disposable e-cigarette nicotine content and e-liquid volume
By Scott Appleton , Helen Cyrus‑Miller, Ryan Seltzer, Karin Gilligan and Willie McKinney Abstract: Inaccurate labels on some e-cigarette products […] Read More
2 min. read
Lucy Goods Submits PMTAs for 42 Nicotine Products
Lucy Goods has submitted premarket tobacco product applications (PMTAs) to the U.S. FDA seeking marketing authorization of 42 of its […] Read More
7 min. read
Watch Your Mouth: What the Nicotine Industry Can’t (and Could) Say About Harm Reduction
By Cheryl K. Olson, Sc.D. Surveys show that the public perceives nicotine as the devil behind most of the cancer […] Read More
1 min. read
Keller and Heckman’s E-Vapor and Tobacco Law Symposium
We will be presenting at Keller & Heckman’s E-Vapor and Tobacco Law Symposium. We join our colleagues and experts from […] Read More
7 min. read
Who D’Ya Think You Are? Your business from the regulators’ perspectives
By Willie McKinney and Cheryl K. Olson Let’s do a thought experiment. Imagine–some of this may sound familiar–that you’re one […] Read More
3 min. read
From MDO to new hope: Could FDA revisit your PMTA?
By Willie McKinney, Ph.D., D.A.B.T. Potential implications of FDA’s October 7, 2021 rescission of its Marketing Denial Order (MDO) issued […] Read More
7 min. read
The FDA gifted you a PMTA deficiency letter … what’s your strategy?
By Willie McKinney and Cheryl K. Olson “I read it. And I thought it was over.” Anne* held the letter […] Read More
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