Headlines Tagged with FDA — 9,763 headlines found
Tamara Koval, who worked at the company...was a co-author of the company’s protocol used to run the studies globally. When she highlighted an irregularity in one of the studies, Koval said, Philip Morris excluded her from meetings.
Dec 20, 2017 Reuters
added Dec 20, 2017 22:46
Monday, six styles of Camel Snus became the first Reynolds American Inc. tobacco products to enter the Food and Drug Administration review process for gaining modified-risk status. Reynolds submitted modified-risk tobacco product applications April 3.
Dec 19, 2017 Winston-Salem (NC) Journal
added Dec 20, 2017 22:12
the world’s biggest multinational tobacco companies seem poised to save many consumers in future, kill millions of them in the meantime and, through multibillion-dollar mergers, become even more powerful. Put that in your pipe and smoke it.
Dec 19, 2017 The Economist
added Dec 20, 2017 15:32
[FDA]...may give approval to Philip Morris to start selling IQOS, its HNB product, in early 2018. That will gall Big Tobacco’s many critics. But it is foolish and puritanical to withhold alternatives that could help save lives which would otherwise be los
Dec 19, 2017 The Economist
added Dec 20, 2017 15:31
On December 18, 2017, FDA filed for substantive scientific review six Modified Risk Tobacco Product (MRTP) Applications from R.J. Reynolds Tobacco Company for the following smokeless tobacco products: Camel Snus Frost Camel Snus Frost Large Camel Snus Me
Dec 18, 2017 FDA - Food and Drug Administration
added Dec 19, 2017 04:30
accepted, and filed for substantive review, 18 Modified Risk Tobacco Product (MRTP) applications covering 6 styles of Camel Snus.
Dec 18, 2017 Reynolds American (RAI)
added Dec 18, 2017 16:58
GLANTZ: Letter to FDA protesting public comment period for IQOS; says comment period should be 180 days after full application is posted
Lauren Lempert and I submitted this letter to Mitch Zeller... We are writing to complain about the public comment process for the above-referenced docket on Philip Morris’s modified risk tobacco product applications (MRTPA) for IQOS. The initial June 1
Dec 12, 2017 Center for Tobacco Control Research and Education (UCSF)
added Dec 16, 2017 20:37
The rise in use of non-traditional tobacco products documented by the survey, as well as increases in little cigar usage among older teens, should be all the motivation the [FDA] needs to finish the process they started in 2016 and fully regulate all toba
Dec 14, 2017 Truth Initiative (American Legacy Foundation)
added Dec 16, 2017 18:10
In the 20th century, tobacco use killed an estimated 100 million people — more than both world wars combined. Most of those smokers had no idea what they were doing to themselves. Tobacco’s deadliness was exposed more than 50 years ago, and a war on smok
Dec 14, 2017 Washington Post
added Dec 16, 2017 17:46
we are proposing meaningful actions to advance our new, comprehensive approach to nicotine and the regulation of combustible cigarettes. These efforts include an Advance Notice of Proposed Rulemaking asking critical questions related to our pursuit of reg
Dec 14, 2017 FDA Blogs
added Dec 16, 2017 17:21