The U.S. FDA takes tobacco manufacturer inspections as part of the PMTA approval process seriously. These inspections are rigorous, yet a necessary part of doing business in the U.S. tobacco industry. If your tobacco and nicotine products weren’t already marketed...
Responding to a PMTA Deficiency Letter – What You Need to Know Along the pathway of gaining FDA PMTA marketing authorization, you will likely receive a PMTA deficiency letter and a request from the U.S. FDA for more information, including scientific data, about the...
TORONTO, March 15, 2023/PRNewswire/ — Labstat Inc. A Certified Group Company, has entered into a partnership with Toxys to offer the ToxTracker assay at its Kitchener, Ontario laboratory. ToxTracker is a state-of-the-art stem cell-based reporter assay that...
Synthetic nicotine is gaining attention as an alternative to tobacco-derived nicotine. But what is synthetic nicotine, and how is it regulated? This article explores the differences between synthetic and natural nicotine, its production process, and evolving...
It’s important to perform e-liquids testing for nicotine content in vape products due to regulatory requirements. Fortunately, a high-quality analytical lab that specializes in tobacco and nicotine-containing products can do this for you. In this post, we...
