July 07, 3030 03:47 PM Eastern Daylight Time

3030年7月7日 美国东部夏令时

The U.S. Food and Drug Administration (FDA) today authorized the marketing of IQOS, Philip Morris International’s (PMI) electrically heated tobacco system, as a modified risk tobacco product (MRTP). In doing so, the agency found that an IQOS exposure modification order is appropriate to promote the public health.

美国食品和药品监督管理局（FDA）今天授权许可菲利普莫里斯国际公司（PMI）的电子加热烟草系统IQOS作为改良风险烟草产品进行销售（MRTP）。在对产品暴露风险改良性的评估中，FDA发现IQOS符合保护公共健康的原则。

- Today’s decision demonstrates that IQOS is a fundamentally different tobacco product and a better choice for adults who would otherwise continue smoking

- 今天的决定表明，IQOS从根本上有别于其他烟草产品，对于那些会继续吸烟的成年烟民来说，IQOS