What is VTA?
The Vapor Technology Association represents the e-liquid manufacturers, device manufacturers, wholesalers, distributors, vape shop owners, small business owners and entrepreneurs who have developed innovative and quality vapor products, providing adult consumers with a better alternative to traditional combustible products. VTA and its members are leaders in the vapor community, promoting small businesses and job growth, responsible public policies and regulations, and a high standard of safety within the industry.

Why should I join VTA?
VTA serves as the leading advocate for manufacturers, wholesalers, suppliers, vape shop owners, and small business owners in the vapor technology industry who not only continue to develop new technologies for the benefit of public health, but also promote small businesses and job growth across the country. VTA and its leadership bring sound policy and a rational perspective to the industry and a responsible approach to the public policies that impact it.

Who are VTA’s Members and How Do I Join?
Innovation in the vapor technology industry is driven by small and mid-size business owners in communities across this country. VTA’s members include industry leading device manufacturers, e-liquid manufacturers, distributors, wholesalers, vape shops, flavor companies, suppliers, importers, and independent state vapor associations.

VTA provides numerous ways for interested companies from every sector of the vapor community to participate in our effort. We have established membership dues that are accessible and that will enable us to provide the highest quality of service to our member companies.

If you are interested in learning more and joining, go to our membership page!

Why is the FDA’s approach to regulating vapor products misguided?
The Tobacco Control Act of 2009 was written in response to the public health crisis generated by combustible cigarettes at a time when vapor products were virtually unknown. Nevertheless, FDA requires pre-market review of all products. By applying the same requirements and predicate date – February 15, 2007 – to current vapor products, the FDA’s rules will effectively eliminate e-cigarettes as an anti-smoking alternative, quashing the first game-changing technology in the ongoing campaign to reduce cigarette smoking.

Furthermore, by treating vapor products like traditional combustible tobacco cigarettes, the FDA does not address the need for responsible regulation of vapor products independent of the tobacco industry. E-cigarettes constitute an entirely new technology and should be treated as such. But, in the years since the implementation of the Deeming Regulation, the FDA has failed to develop any innovative approach to regulating a 21st century technology.

Why should the FDA treat vapor products differently than combustible cigarettes?
According to a vast and growing body of peer-reviewed scientific research, responsibly manufactured e-cigarettes are not only a safer alternative to traditional combustible products, but they also provide many individuals with a viable path to reduce tobacco smoking and even quit altogether. Considering that the National Health Service of the United Kingdom promotes e-cigarettes as one of their smoking cessation tools and now has vape shops opening inside National Health System hospitals speaks volumes about how far behind the U.S. is in recognizing the potential for vapor products.

What effect will the FDA’s rules have on small and mid-size businesses?
Innovation in the vapor technology industry is driven by small and mid-size business owners in communities across this country. The FDA’s misguided, “one size fits all” approach will ensure that only big tobacco survives. Essentially, the FDA is punishing small business owners, entrepreneurs and innovators in the vapor technology space for the past sins of the tobacco industry.