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University of California, San Francisco - Center for Tobacco Control Research & Education - Postdoctoral Fellowships

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Last checkedJun 25, 2026

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FDA’s draft guidance on Principles for Designing and Conducting Tobacco Product Perception and Intention Studies appropriately highlights the importance of determining whether consumers understand the risks of new tobacco products and modified risk claims

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The supplemental modified risk tobacco product application for IQOS 3 does not adequately address new published research and information on emissions of HPHCs and other toxic substances in IQOS aerosol and does not demonstrate benefits to individual or population health, so FDA should not issue an exposure modification MRTP order for IQOS 3

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The supplemental modified risk tobacco product application for IQOS 3 (s MRTPA) does not address new published research and information on the risks to vascular endothelial function from exposure to IQOS aerosol and does not demonstrate benefits to individual or population health.

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The supplemental modified risk tobacco product application for IQOS 3 (s MRTPA) does not adequately address new published research and information on the appeal of IQOS 3 to youth, consumer perceptions of IQOS 3, or the likelihood that the proposed labeling and marketing will mislead consumers, especially youth. The s MRTPA also does not demonstrate benefits to individual or population health. Therefore, FDA should not issue an MRTP order for IQOS 3.

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