Advancements and Challenges of Cigar Science, Testing and Regulation: A Review

R. Abrokwah, Rana Tayyarah
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Abstract

Summary On May 10, 2016, the U.S. Food and Drug Administration (FDA) published a Final Rule that extended its regulatory authority to all tobacco products, including e-cigarettes, cigars, hookah and pipe tobacco (Deemed Products). Effective August 8, 2016, this decision greatly expanded the scope of tobacco products being regulated by FDA and introduced significant testing challenges that need to be addressed. The major challenge for cigars in particular is testing as well as generation of accurate and reliable data, in the absence of certified reference products and standardized methodology for a product category with significant complexity and high inherent variability. In this article, we provide an overview of recent studies as well as active opportunities and on-going challenges associated with regulating and testing cigars. To the best of our knowledge, this is the first comprehensive review of non-clinical research for this product category (cigars). We are therefore convinced that, tobacco scientists and farmers, analytical chemists, cigar consumers, tobacco legal counsels, state and federal regulatory authorities will find this review beneficial and insightful.
雪茄科学、检测和法规的进展与挑战:综述
2016年5月10日,美国食品药品监督管理局(FDA)发布了一项最终规则,将其监管权限扩展到所有烟草产品,包括电子烟、雪茄、水烟和烟斗烟草(视同产品)。该决定于2016年8月8日生效,大大扩大了FDA监管烟草制品的范围,并引入了需要解决的重大测试挑战。对于雪茄来说,主要的挑战是测试和生成准确可靠的数据,因为没有经过认证的参考产品和标准化的方法来衡量一个具有显著复杂性和高度内在变异性的产品类别。在这篇文章中,我们提供了一个概述,最近的研究以及积极的机会和持续的挑战相关的监管和测试雪茄。据我们所知,这是第一次对这类产品(雪茄)的非临床研究进行全面审查。因此,我们相信,烟草科学家和农民、分析化学家、雪茄消费者、烟草法律顾问、州和联邦监管当局将发现这一审查有益而有见地。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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