Last week’s announcement from FDA regarding the authorization of on! PLUS was very encouraging....
Inside FDA’s ENDS Roundtable: What Small Manufacturers Need to Know Now
On February 10, 2026, FDA’s Center for Tobacco Productsconvened a full-day Small Manufacturer ENDS PMTA Roundtable. The objective was straightforward but significant: hear directly from small manufacturers and clarify what FDA expects across the...
Results - 110 Blogs
For much of the past decade, the US nicotine and ENDS marketplace has operated in a state of...
In 2025, Sweden achieved something virtually unheard of elsewhere: it became and may soon be...
The inaugural PouchEx 2025 conference, dedicated exclusively to nicotine pouches, was a niche event...
The 2025 Food and Drug Law Institute (FDLI) Tobacco and Nicotine Conference delivered something the...
When FDA deployed the “fatal flaw” concept during ENDS PMTA reviews, it was seen by many as a...
The 2025 CORESTA Product Science and Product Technology (PSPT) Conference brought together...
The 2025 Global Tobacco and Nicotine Forum (GTNF), held in Brussels, brought together policymakers,...
By Paul Hardman, Chemistry Consultant at Broughton With expert regulatory commentary from Lilian...
If you have a specific question for one of our scientific or regulatory experts, get in touch with a member of our team today.
