USA
-
Evolving Story of Vaping Regulations in the U.S.: 2024’s Pivotal Year
If you’ve been following the news lately, it feels like vaping is constantly making headlines, doesn’t it? The FDA, politicians, and industry players are all locked in this ongoing tug-of-war, trying to figure out how to handle these controversial products. And honestly, it’s a bit overwhelming to keep track of…
Read More » -
Will Vapes Be Saved Again in the US?
The vaping industry finds itself at another critical juncture, with increasing regulation and public scrutiny threatening to reshape its future. As debates around environmental compliance, youth access, and health concerns dominate headlines, many are asking: Can vapes survive this storm, or will they be saved once more by decisive action?…
Read More » -
FDA Greenlights Vuse Alto Tobacco-Flavored Vapes for Marketing
Last week marked a significant milestone for Vuse Alto, as the FDA granted marketing authorization for its tobacco-flavored vapes. This decision underscores the agency’s recognition of these products as a potential aid for adults looking to quit traditional cigarettes. Unlike full FDA approval, this authorization allows Vuse Alto to be…
Read More » -
Philip Morris International Boosts Zyn Production with $600 Million Investment in U.S.
Philip Morris International (PMI) is ramping up its commitment to reducing cigarette smoking in the U.S. by investing $600 million to build a new factory in Aurora, Colorado. This facility aims to meet the soaring demand for Zyn nicotine pouches among American consumers. With the plant set to start operations…
Read More » -
The Impact of PMTA Regulations on Small Vape Companies in the US Market
The US vape market is currently facing significant challenges due to the Premarket Tobacco Product Application (PMTA) process, implemented by the Food and Drug Administration (FDA). This regulatory pathway is crucial for new tobacco products aiming to enter or remain on the market, demanding a high level of scientific evidence…
Read More » -
FDA Faces Criticism Over E-Cigarette Regulation in the United States, Public Hearing Set for June
On May 7th, according to Courthouse News, Senator Dick Durbin, chairman of the Senate Judiciary Committee, publicly criticized the FDA for failing to effectively prohibit the unauthorized sale of e-cigarettes. The Senate Judiciary Committee in the United States is set to hold a crucial public hearing on the issue of…
Read More » -
New Utah Law Threatens Local Vape Shops with Closure
The Controversial Flavor Ban In Utah, a recent legislative move to ban flavored e-cigarettes is stirring controversy and fear among local vape shop owners. The law, championed by pediatrician and Senator Jen Plumb, aims to curb the rising trend of vaping among teens by eliminating sweet and fruity e-cigarette flavors.…
Read More » -
Kentucky’s New Anti-Vaping Law Faces Legal Pushback
Constitutional Challenges to Kentucky’s Vaping Legislation In Kentucky, a significant legal challenge has arisen against the state’s new law that targets the sale of vaping products. Set to take effect on January 1, the law permits only the sale of vaping products that have been authorized or are under review…
Read More » -
SMOK’s Legal Challenge Against FDA: Navigating the Complex Intersection of Vaping Innovation and Public Health Regulations
Chinese Vape Brand SMOK Appeals Against US FDA’s Marketing Denial Order On January 18, Shenzhen IVPS Technology Co., Ltd., the parent company of the SMOK brand, announced that it has filed an appeal with the United States Fifth Circuit Court of Appeals against the US Food and Drug Administration (FDA)’s…
Read More » -
FDA Rejects Bidi Stick – Classic E-Cigarette for U.S. Market
In a significant move on January 22, 2024, the U.S. Food and Drug Administration (FDA) issued a marketing denial order (MDO) to Bidi Vapor LLC for its Bidi Stick – Classic e-cigarette. This product, a closed-system, disposable, tobacco-flavored e-cigarette device, can no longer be marketed or distributed in the United…
Read More »
