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The report argues for non-marginal reform to the FDAs authorization process, to bring at least 4,000 vaping and other safer products to market, meet the statutory 180-day requirement for complementing reviews, and lower barriers to entry by a factor of 10

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The schema will allow for the creation of a class-specific brick to capture product that cannot be immediately placed into an existing brick or products that the industry determines should not be broken out

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