miércoles, 11 de noviembre de 2015

FDA issues first product marketing orders through premarket tobacco application pathway – 10 de Noviembre de 2015 – EEUU

Following a rigorous, science-based review, the U.S. Food and Drug Administration announced today that for the first time it has authorized the marketing of new tobacco products through the premarket tobacco application (PMTA) pathway. This action permits the tobacco products to be sold in the U.S., but does not mean that they are safe or “FDA approved.” All tobacco products are potentially harmful and addictive and those who do not use tobacco products should continue to abstain from doing so.

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