The Keller and Heckman LLP E-Vapor and Tobacco Law Symposium provided in-depth discussions on the...
The FDA’s Authorisation of Zyn: A Robust PMTA in a Changing Landscape
On January 16, 2025, the FDA granted marketing authorisation for Swedish Match’s Zyn nicotine pouches, marking a significant regulatory milestone for the modern oral nicotine market. Given the rapid expansion of this category, many companies may see...
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Nicotine pouches are exciting products that can help support worldwide tobacco harm reduction....
As the global tobacco and nicotine market evolves, nicotine pouches are emerging as a popular...
Broughton welcomes the US Food and Drug Administration’s (FDA) decision to authorize ZYN nicotine...
Navigating FDA and ICH Guidelines: Analytical Testing Validation for Tobacco Products
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Oral nicotine pouches have become a disruptive force in the reduced-risk nicotine product...
Allergies concerns highlights need to meet stringent regulations ~
The tobacco harm reduction (THR) industry is undergoing significant changes, driven by advancements...
~ Why new age verification technology could help solve youth appeal ~
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