The new IQOS 3, Philip Morris International’s (PMI) newer and more advanced electrically heated tobacco system, recently received U.S. Food and Drug Administration (FDA) premarket tobacco product authorization (PMTA) confirming that the device is “appropriate for the protection of public health” and authorizing it for sale in the United States.
The U.S. FDA’S latest decision also said that based on the international survey data it reviewed, the agency found no evidence of increased uptake of IQOS by youth or young adults, while use patterns available for a previously authorized version of IQOS within the U.S. have not raised new concerns regarding product use i…
Keep on reading: U.S. FDA authorizes sale of IQOS 3