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Modified risk tobacco product: Historic FDA decision and lessons for Africa

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Following 43 months of evaluation, the U.S. Food and Drug Administration (FDA) on 7 July authorized the marketing of IQOS in the country, Philip Morris International’s (PMI) electrically heated tobacco system, as a modified risk tobacco product (MRTP). This decision by the U.S. FDA marks the first time the agency has granted MRTP marketing orders for an […]

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