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VTA Statement: Critiques FDA’s Denial of Suorin Device and blu PLUS+ PMTAs

January 19, 2024 by Tony

STATEMENT FROM THE VAPOR TECHNOLOGY ASSOCIATION IN RESPONSE TO CTP’S DECISION TO DENY MARKETING OF SUORIN AND blu PLUS+ E-CIGARETTE PRODUCTS 

WASHINGTON, D.C. – January 19, 2024 – The following statement is attributable to Tony Abboud, executive director of the Vapor Technology Association (VTA):

“Today’s decision by the U.S. Food and Drug Administration (FDA) Center for Tobacco Products (CTP) to issue marketing denial orders (MDOs) for Suorin and blu PLUS+ e-cigarette premarket tobacco applications (PMTAs) is just the latest installment of FDA and CTP’s efforts to implement its de-facto ban on e-cigarettes in the U.S.”

“The constant refrain from CTP is that e-cigarette manufacturers are not providing ‘sufficient scientific evidence’ in their PMTAs, yet CTP refused to answer the Reagan-Udall Foundation’s most fundamental criticism of CTP’s entire regulatory process: that CTP has not clearly articulated what is required to prove what is appropriate for the protection of the public health (APPH) or how it is interpreting what is APPH.”

”Having failed to objectively define this standard while simultaneously using it to deny marketing authorization to critical smoking-cessation and harm-reduction products is a gross overreach for any governmental institution whose mandate is to follow the science. Courts have found that the process has become ‘arbitrary and capricious’ in practice, with CTP leadership choosing on a case-by-case basis how the standard ought to be defined. Meanwhile, companies are simply trying to do the right thing by complying with and adhering to the PMTA process set forth by the FDA.”

“What is most striking is that CTP claims that its denial of Suorin’s PMTAs was because its product promoted ‘continued use and development’ of dependence. If this is the standard, then every nicotine product will fail the bizarre standards of CTP, since nicotine is addictive, which will further CTP’s implementation of a ban on less harmful forms of nicotine and further lock 30 million Americans in the grip of toxic cigarettes.”

“This action by CTP comes on the heels of an earlier MDO against another c-cigarette company and clearly reflects CTP’s steadfast commitment to deny any and all products or devices which Americans can use as a dramatically less harmful alternative to combustible cigarettes.”

“CTP also continues to falsely assert that these products are popular with younger users. FDA’s own data in fact demonstrate a rate of 70,000 out of 28 million, approximately 0.25%. At what point will CTP stop and realize the dramatically low youth rate merits real and thoughtful consideration of the value of e-cigarette products for adults looking for a less harmful alternative to combustible tobacco?”

“Today’s actions of FDA and CTP do nothing to protect public health or help Americans who smoke. VTA once again calls on CTP to reverse course on its bad faith actions and restore scientific integrity to its regulatory and decision-making process. Enough is enough.”

# # #

About VTA: The Vapor Technology Association is the leading industry trade association in the United States whose members are dedicated to sound science-based regulation and selling innovative high-quality vapor products that provide adult smokers with a better alternative to combustible cigarettes. VTA represents the industry-leading manufacturers of vapor devices, e-liquids, and flavorings, as well as the distributors and retailers, including hardworking American mom-and-pop brick-and-mortar retail store owners.

Filed Under: News, Press Releases Tagged With: FDA, MDOsPMTA, vaping association

VTA Statement: Critiques FDA’s Denial of SMOK Device PMTAs

January 16, 2024 by Tony

STATEMENT FROM THE VAPOR TECHNOLOGY ASSOCIATION IN RESPONSE TO CTP’S DECISION TO DENY MARKETING OF SMOK E-CIGARETTE PRODUCTS 

WASHINGTON, D.C. – January 16, 2024 – The following statement is attributable to Tony Abboud, executive director of the Vapor Technology Association (VTA):

“Today’s decision by the U.S. Food and Drug Administration (FDA) Center for Tobacco Products (CTP) to issue 22 marketing denial orders (MDOs) for SMOK e-cigarette premarket tobacco applications further reinforces FDA’s steadfast commitment to its de-facto ban on e-cigarettes in the U.S.”

“For the first time, CTP has denied marketing authorization for purely technological devices that, per CTP’s own announcement, contain no tobacco, no nicotine, no e-liquid, and no flavorings. Still, CTP concluded that the American people couldn’t be trusted with these products because they “have the potential to be used with any e-liquid on the market and available to the consumer, which could include tobacco-flavored and non-tobacco flavored e-liquids.” In other words, CTP will deny Americans any device which allows them to consume nicotine in a manner that is scientifically proven to be dramatically less harmful than combustible cigarettes.”

“Today’s announcement reveals a rapid acceleration of CTP’s efforts remove any and all vaping devices from the market. Predictably claiming its decision was based on science, in actuality it had little to do with the data. CTP blithely asserted that SMOK products are popular with youth e-cigarette users. However, the 2023 National Youth Tobacco Survey (NYTS) data relied on by CTP, revealed the opposite. Not only did the data show another massive decline in youth use of any e-cigarettes (down 60% since 2019 and at a decade low), the data cited actually showed that less than one-tenth of one percent (230,000) of American youth even tried one of the SMOK products CTP just banned. Based on this objectively minute risk, CTP is barring millions of responsible adults from using these popular and technologically innovative products.”

“Like virtually all e-cigarettes, SMOK devices are a critical tool for American smokers looking for a less harmful alternative to smoking deadly cigarettes. CTP’s decision today is a rejection of technological innovation and is the most serious indication yet that it will not stop until all vaping products are eliminated in the U.S.”

“With CTP’s announcement, the VTA is once again renewing its call for CTP to reverse course, actually follow the science, and restore scientific primacy and integrity to its regulatory process.” 

# # #

About VTA: The Vapor Technology Association is the leading industry trade association in the United States whose members are dedicated to sound science-based regulation and selling innovative high-quality vapor products that provide adult smokers with a better alternative to combustible cigarettes. VTA represents the industry-leading manufacturers of vapor devices, e-liquids, and flavorings, as well as the distributors and retailers, including hardworking American mom-and-pop brick-and-mortar retail store owners.

Filed Under: News, Press Releases Tagged With: FDA, MDOsPMTA, vaping association

VTA Announces New Leadership Team

January 11, 2024 by Tony Leave a Comment

VTA’s new leadership is dedicated to advancing the independent vapor industry’s efforts to promote sound science-based regulation that will ensure the future of tobacco harm reduction

WASHINGTON, D.C. – January 11, 2024– The Vapor Technology Association (VTA) today announced the election of new members to its leadership team. The VTA Board of Directors elected Dr. David Johnson, Ph.D, as its new Board President, and elected Charles “Chuck” Melander as its new Treasurer.

“We are proud to welcome both David and Chuck to VTA’s Board and leadership team,” said Tony Abboud, VTA’s Executive Director. “Collectively, David and Chuck bring decades of valuable scientific and regulatory expertise, and bold, visionary leadership to the Vapor Technology Association as we chart the future of tobacco harm reduction and smoking cessation alternatives to cigarettes at the federal and state levels.  I am excited to work with them as we drive our Association’s goals and our core mission of advocating for e-cigarettes as  less harmful alternatives to combustible cigarettes.

Dr. David Johnson

Dr. Johnson is president of VTA member e-LiquidTech, Inc., an industry leading e-liquid and flavor manufacturer and major supplier to the tobacco and vaping industries. Dr. Johnson, a Ph.D in chemistry and analytical chemistry, brings to VTA over 30 years of scientific, regulatory, and management experience, including over 20 years in the tobacco and vape industries at Swedish Match – North America and at Turning Points Brands. Dr. Johnson also serves on the U.S. Food and Drug Administration’s Tobacco Products Scientific Advisory Committee (TPSAC) as a small tobacco industry representative. Dr. Johnson’s extensive range of professional experiences and knowledge will support the scientific and regulatory focus and strategy of the Association. 

“It’s an honor and privilege to be recognized among my peers at VTA’s member companies, and I look forward to serving in my new role leading the Association and serving on VTA’s Executive Committee,” said Dr. Johnson. “We know that we have a lot of work to do, and I’m proud to be a part of this great team that has been leading and will continue to lead the charge to provide equitable access to vaping products as an important harm reduction and health equity tool.”

Chuck Melander

Mr. Melander, the Chief Strategy Officer of VTA member Streamline Vape Co., an industry leading e-liquid company, brings an entrepreneurial mindset, with a long record of brand building, driving radical growth, strategic and long-term planning efforts, and regulatory strategy. With a well-tenured career at Swedish Match and Turning Point Brands, where he served on the Executive Teams that drove rapid growth within the companies, Mr. Melander developed strong expertise in less harmful nicotine alternatives to cigarettes. Mr. Melander, a biochemist by training, has also served as an alternate member of TPSAC. Mr. Melander has an acute understanding of the legal and regulatory framework at both the federal and state levels.

“I am excited to take on this new challenge at VTA and move into a role which allows me to bring my experience in the vaping and tobacco industries to advance commonsense policies which support the broad access for responsible adult use of vaping products,” said Mr. Melander. “I thank the VTA Board for this nomination, and I look forward to working with the rest of the Executive Committee and the Board to advance VTA’s critically important mission.”

“On behalf of the VTA Board, I would also like to thank George Cassels-Smith, CEO of Tobacco Technology Inc and e-LiquidTech, Inc., for the steady and thoughtful leadership he has provided to VTA over the past three years and for the sound guidance he has provided me,” said Tony Abboud.  Under Mr. Cassels-Smith’s leadership, VTA was able to weather the organizational challenges presented by the pandemic, restore VTA’s footing as a leading voice for rational science-based regulation of less harmful nicotine products, and establish a strong direction for the future.  “The vaping industry owes Mr. Cassels-Smith a debt of gratitude for his past and continuing commitment to VTA and our common mission.”

Dr. Johnson and Mr. Melander assumed their new roles in December and, together with Jon Glauser, who also was re-elected by the Board as VTA’s Secretary, will serve on VTA’s Executive Committee.

David Johnson
Chuck Melander

# # #

About VTA: The Vapor Technology Association is the leading industry trade association in the United States whose members are dedicated to sound science-based regulation and selling innovative high-quality vapor products that provide adult smokers with a better alternative to combustible cigarettes. VTA represents the industry-leading manufacturers of vapor devices, e-liquids, and flavorings, as well as the distributors and retailers, including hardworking American mom-and-pop brick-and-mortar retail store owners.

Filed Under: News, Press Releases Tagged With: vaping association

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