The U.S. Food and Drug Administration (FDA) has just allowed the marketing of two new tobacco products from Lorillard Inc and denied the marketing of four others. This is the first time that the agency has used it's authority to regulate tobacco products since the Family Smoking Prevention and Tobacco Control Act of 2009, which gave the FDA the right to regulate tobacco products with the substantial equivalence (PE) pathway. The U.S. Food and Drug Administration said that tobacco products introduced or changed after Feb. 15, 2007 have to be reviewed by the agency...
via Health News from Medical News Today Read More Here..
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