Dr Paul Marshall has joined the Nerudia team as a regulatory principal. His role will be to support customers with medicinal, PMTA and TPD projects. Read More
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Philip Morris International has filed its highly anticipated MRTP application with the FDA. The company is seeking the right to make a health claim on its iQOS heat-not-burn vaporizer.Read More
The rumors are unfounded. The FDA will publish a rule change today that will address how it "refuses to accept" premarket tobacco applications. A meaningless notion for most vapor companies.Read More
E-cigarettes can explode. How to prevent tragedies from happening.Read More
Flavors, manufacturing and ethics have proved a winning formula for Five Pawns.Read More
Writing on his blog, The counterfactual, Clive Bates says that the US Food and Drug Administration’s deeming rule, which came into force on Monday, spells the end of innovation.Read More
Altria’s Nu Mark has told the US Food and Drug Administration that its pre-market tobacco application requirements for e-cigarettes are unduly burdensome, unnecessary, and beyond the scope of the agency’s jurisdiction under the Read More
Dr. Michael Siegel, a professor in the Department of Community Health Sciences, Boston University School of Public Health, said the FDA had drastically underestimated the costs of the regulations and not attempted to quantify the Read More
Vapor industry manufacturers are finding more than a few faults with the FDA regulations, especially the seeming lack of consideration from the industry input the regulatory agency so desperately sought.Read More
The U.S. House Appropriations Committee, on April 19, approved an amendment to the Agriculture Appropriations bill offered by Rep. Tom Cole (R-OK) and Rep. Sanford Bishop (D-GA), that would modify the predicate date for vapor Read More