Broughton's Chief Scientific and Regulatory Officer, Dr Nveed Chaudhary has published an article on the recent FDA announcement on synthetic nicotine with the leading sector publication Tobacco Reporter.
Dr Nveed Chaudhary has written an article explaining the recent Food and Drug Administration (FDA) announcement to regulate synthetic nicotine and what this means for the next-generation nicotine delivery (ENDS) industry. The industry has been debating how governments will respond to regulating synthetic nicotine products for some time. The new regulation was passed on March 15th as part of a U.S. lawmaker’s long-term spending bill signed into law by President Joe Biden.
Manufacturers of synthetic nicotine in products such as vapes, heated products and oral nicotine pouches need to act immediately. They will have 60 days from March 15 to submit a Premarketing Tobacco Product Application (PMTA) dossier to keep their products on the US market.
In this article Nveed discusses:
You can read the full article here
To learn more about the new FDA regulations and submission requirements for synthetic nicotine for ENDS in the US market, contact us to book a meeting and talk to one of our Regulatory Service team members.
Broughton have deep CRO capabilities and an experienced team of scientific and regulatory professionals to manage full service global regulatory projects. Our knowledge of global regulatory pathways offers significant insights that can be incorporated into your project plans. Our mission is to accelerate safer nicotine-delivery products to market; creating a smoke-free future.
Book a meeting with us today to discuss your requirements.