Tobacco product manufacturers are required to comply with certain requirements under Section 904(a) of the Federal Food, Drug and Cosmetic Act (FD&C Act). What does this have to do with vape shops...
Nicotine

Nov 26, 2019 | Published by Andrew Mooney
Nicotine
ENDS US 2019 is the ideal place to keep up with the ever-changing knowledge base required to operate in the nicotine products industry; the Advisory Board has worked hard to put together an exemplary agenda packed with opinion leaders across the legal, regulatory and scientific arenas and they will all give meaningful insights into what is happening in the industry and where it might go in 2020 and beyond.
Broughton is exhibiting at the event in Arlington, Virginia on 10-11th December along with other industry-leading companies supporting next generation nicotine products. Come along to discuss how we can help with ENDS regulatory challenges. It will also be an opportunity to discuss some of the recent confusing news stories and remind ourselves that vape products are 95% safer than smoking.
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Tobacco product manufacturers are required to comply with certain requirements under Section 904(a) of the Federal Food, Drug and Cosmetic Act (FD&C Act). What does this have to do with vape shops...
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The US Food and Drug Administration (FDA) has published final guidance regarding Enforcement Priorities for Electronic Nicotine Delivery Systems (ENDS), detailing how they intend to prioritize...
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Yesterday I attended the UKVIA reception at the House of Commons to launch this year's VApril campaign. It was a drizzly arrival at Parliament, but was soon brightened by seeing so many old friends...