审查 FDA 监管消费品的(安全)证明标准,以及如何将公认安全标准应用于化妆品。

IF 3 4区 医学 Q1 MEDICINE, LEGAL Regulatory Toxicology and Pharmacology Pub Date : 2024-03-15 DOI:10.1016/j.yrtph.2024.105603
George A. Burdock
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引用次数: 0

摘要

2022 年化妆品管理现代化法案》(MoCRA)修订了《食品、药品和化妆品法》 (FDCA),将化妆品的安全证明标准(更多地被称为 "安全标准")提高到 "合理确 定......[的]......安全 "的标准,这一标准与食品成分的标准相同。食品及药物管理局监管的各类产品(如化妆品、膳食补充剂、食品配料和食品本身)的安全性证明标准各不相同。本手稿介绍了各种证明标准、标准之间的本质区别、达到特定标准所需的关键要素,并将这些标准与 "优势证据 "或 "排除合理怀疑 "等更熟悉的法律术语进行了比较。这些产品类别的举证标准还根据获得 "安全 "地位的门槛的提高进行了排序。最后,本手稿提出了如何达到 "合理确定安全"(或 "合理确定无害")这一高标准的要求。
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Review of the standards of proof (of safety) for FDA regulated consumer products and how the generally recognized as safe criteria could be applied to cosmetics

The Modernization of Cosmetics Regulation Act of 2022 (MoCRA) amends the Food, Drug and Cosmetic Act (FDCA), elevating the standard of proof of safety (better known as a “safety standard”) for cosmetics to the standard of a “reasonable certainty … [of] … safe.”a standard equal to that of food ingredients. The standards of the proof of safety differ for various classes of FDA-regulated product categories e.g., cosmetics, dietary supplements, food ingredients and food itself. This manuscript describes the various standards of proof, the essential differences between the standards, key elements required to achieve a particular standard and, compares the standards to more familiar legal terms such as “a preponderance of the evidence” or “beyond reasonable doubt.” The standards of proof for these product categories are also ranked according to increasing threshold for achievement of “safe” status. Lastly, this manuscript suggests how the requirements for the high standard of a “reasonable certainty of safe” (or “reasonable certainty of no harm”) might be met.

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来源期刊
CiteScore
6.70
自引率
8.80%
发文量
147
审稿时长
58 days
期刊介绍: Regulatory Toxicology and Pharmacology publishes peer reviewed articles that involve the generation, evaluation, and interpretation of experimental animal and human data that are of direct importance and relevance for regulatory authorities with respect to toxicological and pharmacological regulations in society. All peer-reviewed articles that are published should be devoted to improve the protection of human health and environment. Reviews and discussions are welcomed that address legal and/or regulatory decisions with respect to risk assessment and management of toxicological and pharmacological compounds on a scientific basis. It addresses an international readership of scientists, risk assessors and managers, and other professionals active in the field of human and environmental health. Types of peer-reviewed articles published: -Original research articles of relevance for regulatory aspects covering aspects including, but not limited to: 1.Factors influencing human sensitivity 2.Exposure science related to risk assessment 3.Alternative toxicological test methods 4.Frameworks for evaluation and integration of data in regulatory evaluations 5.Harmonization across regulatory agencies 6.Read-across methods and evaluations -Contemporary Reviews on policy related Research issues -Letters to the Editor -Guest Editorials (by Invitation)
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