USA
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WHO EXIT BY THE UNITED STATES FORCES FCTC ACCOUNTABILITY: A TURNING POINT FOR ASIA PACIFIC POLICY
Wellington, New Zealand, 9 February 2026. The Coalition of Asia Pacific Tobacco Harm Reduction Advocates (CAPHRA) calls on Asia-Pacific governments to review WHO Framework Convention on Tobacco Control (FCTC) following US withdrawal from WHO (22 January 2026) and New Zealand Foreign Minister Winston Peters questioning continued funding. The US cited…
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The Real Difference Between a Medical Marijuana Card and a Recreational ID
If you live in Virginia, you may have noticed an ongoing conversation about cannabis access and what it takes to use it legally. While recreational cannabis laws are evolving, many people still wonder whether they need a medical marijuana card VA or if a recreational ID is enough. The truth is…
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A Milestone for Nicotine Pouches: FDA Approves 20 ZYN Products
Big news from the U.S. Food and Drug Administration (FDA): after rigorous scientific review, the agency has officially approved 20 ZYN nicotine pouch products for sale through the Premarket Tobacco Product Application (PMTA) pathway. This marks a historic moment—it’s the first time nicotine pouches, those tiny synthetic fiber bags packed…
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CAPHRA EXPOSES ANTI-TOBACCO FUNDING SCANDAL: VIOLATIONS OF INTERNATIONAL AND U.S. LAW ALLEGED
The Coalition of Asia Pacific Harm Reduction Advocates (CAPHRA) today calls attention to a growing international scandal involving prominent anti-tobacco organisations and their alleged misuse of funds to manipulate policies in developing countries, potentially violating both local laws and the U.S. Foreign Corrupt Practices Act (FCPA). Recent investigations have revealed…
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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…
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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?…
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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…
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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…
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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…
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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…
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