Marketing Of IQOS Authorised By United States FDA As A Modified Risk Tobacco Product | Sahara Reporters

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Marketing Of IQOS Authorised By United States FDA As A Modified Risk Tobacco Product | Sahara Reporters
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Marketing Of IQOS Authorised By United States US_FDA As A Modified Risk Tobacco Product | Sahara Reporters The agency found that an IQOS exposure modification order is appropriate to promote public health. READ MORE:

The United States Food and Drug Administration has authorised the marketing of IQOS, Philip Morris International’s electrically heated tobacco system, as a modified risk tobacco product , a report by allafrica.com, has said.

The report further stated that the product, scientific research had shown, posed almost no risk for users’ health. This decision follows a review of the extensive scientific evidence package PMI submitted to the FDA in December 2016 to support its MRTP applications.

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