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CBA TO FDA: Urgent action required on CBD regulation

机译:CBA至FDA:CBD规则所需的紧急行动

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The Consumer Brands Association on July 22 renewed its call for government action on cannabidiol (CBD) regulation in letters addressed to Janet Woodcock, MD, acting commissioner of the Food and Drug Administration, and Senator Ron Wyden of Oregon, chairman of the Senate Committee on Finance. The letter to Dr. Woodcock from Betsy Booren, CBA's senior vice president, regulatory affairs, stated the "FDA stance on CBD products is not working" and a regulatory framework for CBD products is "needed now to protect consumers, ensure product safety and transparency, establish guardrails for legal product innovation and distribution in interstate commerce, and provide the clarity needed for manufacturers of these products." Ms. Booren summarized the FDA stance as holding fast to a position that CBD-containing dietary supplements and foods may not be marketed under the exclusionary clauses of the Food, Drug, and Cosmetics Act (FDCA) and that the use of these products may present serious safety concerns.
机译:7月22日的消费品牌协会将其呼吁对汉德·伍德科克,MD,食品和药物管理局的janet Woodcock,MD,参议院委员会主席的俄勒冈州参议员罗恩·威登参议员致电金融。来自Betsy Booren博士的信CBA的高级副总裁,监管事务副总裁博士致函“CBD产品上的FDA姿势不起作用”,即“现在需要为保护消费者提供CBD产品的监管框架,确保产品安全和透明度,建立法律产品创新和分销的守卫,在州际商务方面,提供了这些产品制造商所需的清晰度。“ Booren女士总结了FDA姿态,因为在食品,药物和化妆品法案(FDCA)的排他性条款下,含有CBD膳食补充剂和食品可能无法销售的含有CBD的膳食补充剂和食品的地位,并且可能存在这些产品的使用严重的安全问题。

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    《Food Business News 》 |2021年第12期| 22-22| 共1页
  • 作者

    Jay Sjerven;

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