登录查看更多内容

Quarterly Newsletter: Tobacco & Nicotine

Labstat International Inc.

So The World Can Trust In What It Consumes?

发布日期: 2025年2月27日

+ 关注

Top Industry Headlines

U.S. FDA Authorizes Marketing of 20 ZYN? Nicotine Pouch Products after Extensive Scientific Review
Generational Tobacco Ban Likely to Become Law in United Kingdom
Global e-Cigarette Market to Reach $23.15 Billion by 2029
U.S. FDA Issues "Validation and Verification of Analytical Testing Methods Used for Tobacco Products" to Aid Application Submissions
California Lawmakers Propose Bill that Would Ban Sale of Disposable e-Cigarettes

Our scientists are presenting three posters next month at the Society of Toxicology 64th Annual Meeting and ToxExpo in Orlando:

? Development of Enhanced Collection and Extraction Techniques for In Vitro Toxicology Testing of Next Generation Nicotine Products (Pavel Kosachevsky, Bonnie Coffa, Katarina Aleksa, Dan Iorgulescu)

? Assessment of Nuclei-Based Cytotoxicity Measurement as an Alternative to Bead-Based Methods in Flow Cytometry (Sean Oh, Dong Ma, Landen Power, Katarina Aleksa)

? Comparative Analysis of In Vitro Testing for Oral Nicotine Products Versus Combustible Cigarettes: Implications for Public Health and Harm Reduction Strategies (Bonnie Coffa, Katarina Aleksa)?

Join us during the poster sessions or in booth #1350 to discuss our research and talk about your PMTA needs!

Dr. Peter Gibbons, Labstat Director of Business Development for Europe, recently spoke with 2FIRSTS about key issues in the nicotine industry, including:

The need for a standardized global method to differentiate synthetic and tobacco-derived nicotine.
Ongoing debates surrounding synthetic nicotine.
Evolving global regulations and their impact on the industry.

Read the article for Dr. Gibbons' insights.

Read The Article

Tips from Experts for Preparing a Successful U.S. FDA PMTA

PMTA submissions require a tremendous amount of data presented in the proper format. Preparing a submission is difficult enough without risking a denial due to an avoidable oversight.?

Our team provides guidance for a successful submission, including the 11 specific sections the U.S. FDA requires in 21 CFR 1114.7.?

Get The Tips

Labstat offers ISO 17025-accredited Crop Protection Agent (CPA) testing to help you meet Maximum Residue Limits (MRLs) and Good Agricultural Practice (GAP) standards.

Our robust testing capabilities include: