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Modified Risk Tobacco Products The modified risk tobacco product (MRTP) pathway is outlined in the 2009 Family Smoking prevention and Tobacco Control Act [and] allows companies to submit applications for the FDA to evaluate whether a tobacco product may be sold or distributed for use to reduce harm or the risk of tobacco-related disease associated with commercially marketed tobacco products. The FDA maintains that the products authorized to be marketed with this claim are neither safe nor FDA-approved

The panel rejected the argument that scientific publications presented as evidence in dispute settlement proceedings can only be validly considered by a panel if the complete underlying research data is also made available.[17] Because public health authorities rely on scientific publications to support their actions, this evidentiary finding is important

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