PMTA Updates

Thousands of manufacturers and importers submitted premarket tobacco product applications (PMTAs) to the Food and Drug Administration by the Sept. 9, 2020, deadline to continue selling their products in the United States. How have these applications fared? Who will remain in the market and who willl exit? Keep up with the latest developments in market authorizations in this dedicated section of our website.

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Licensed to Thrive

There may soon be a licensed medicinal inhaled nicotine product on the market with Qnovia.

Certified Medicine

More than a year after the U.K.’s MHRA guidance, there are still no medicinal vapes on the market.

Head in the Clouds

A vaping industry veteran uses some time-tested adages to reflect on his 11 years in the space.

Behind Schedule

Two branches of U.S. government have the power to change marijuana’s Schedule I status.

House of Cards

If you improve the way that you implement bad policies, you are still left with bad policies.

The first issue of 2023 delves into electronic nicotine delivery system (ENDS) products and their potential to be approved as medicinal products. Also, how flavor bans impact manufacturers, Clive Bates covers innovation, Chris Howard looks back on vaping sector, Willie McKinney breaks down marijuana scheduling and Troutman Pepper attorneys talk taxes.

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