I apologize if this is being discussed somewhere else and I missed it but I just noticed this a few minutes ago. Apparently this happened today? Can someone who has more information that me explain if this could possible affect us? I'm a noob and am not entirely sure if "ecigs" would be considered pre-07 or post. The fact that the words "or other tobacco products" makes me think pvs are a possible target.
FDA demands review of newer tobacco products - Health - Addictions - msnbc.com
RICHMOND, Va. — The Food and Drug Administration says it must review tobacco products that were introduced or changed after February 2007 in order for companies to keep selling them.
The agency on Wednesday issued guidance to the tobacco industry outlining how to apply for review.
Tobacco makers have until March 22 to prove that the cigarettes or other tobacco products are "substantially equivalent" to ones commercially available before Feb. 15, 2007. That mean the ingredients and design are similar and do not raise different public health concerns -- otherwise they may be prohibited from sale.
The FDA won the authority in 2009 to regulate tobacco products.
"This specific part of the law is meant to ensure that new tobacco products are evaluated by the FDA before they are cleared to enter the marketplace," Dr. Lawrence Deyton, head of the FDA's tobacco center, said in a statement.
FDA demands review of newer tobacco products - Health - Addictions - msnbc.com
RICHMOND, Va. — The Food and Drug Administration says it must review tobacco products that were introduced or changed after February 2007 in order for companies to keep selling them.
The agency on Wednesday issued guidance to the tobacco industry outlining how to apply for review.
Tobacco makers have until March 22 to prove that the cigarettes or other tobacco products are "substantially equivalent" to ones commercially available before Feb. 15, 2007. That mean the ingredients and design are similar and do not raise different public health concerns -- otherwise they may be prohibited from sale.
The FDA won the authority in 2009 to regulate tobacco products.
"This specific part of the law is meant to ensure that new tobacco products are evaluated by the FDA before they are cleared to enter the marketplace," Dr. Lawrence Deyton, head of the FDA's tobacco center, said in a statement.