Stakeholders will on April 12 have an opportunity to verbally comment on the agency’s proposed rule. Read More
Tags : U.S. Food and Drug Administration
More bureaucrats and task forces are unlikely to addresses the Center’s shortcomings, say critics. Read More
More bureaucrats and task forces are unlikely to addresses the Center’s shortcomings, say critics. Read More
More bureaucrats and task forces are unlikely to addresses the Center’s shortcomings, say critics. Read More
Stressing its need for resources, the centers also suggests user fees on e-cigarettes.Read More
The Inspector General suggests that the agency improve its data collection and transparency to be better factually. Read More
The e-cigarette manufacturer believes that the marketing denial was substantively and procedurally flawed. Read More
The agency is not targeting the vaping products most popular with young people, according Truth Initiative.Read More
Litigation
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PMTA
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U.S. FDA
Second Chance: MDO Legal Win Presents Opportunity
How companies can make the most of a recent ruling requiring FDA to reassess 1,000s of PMTA rejection notices.Read More
The industry group says Triton’s MDO appeal involves issues of ‘exceptional importance.’Read More
