Home»News»Federal News»One day after notice by Hartland, Wisconsin, FDA delays Tobacco “Deeming” Regulation

One day after notice by Hartland, Wisconsin, FDA delays Tobacco “Deeming” Regulation

7
Shares
Pinterest Google+

Announces new plan to “shift trajectory” of disease, death

(Washington, D.C.) – The Electronic Vaping Coalition of America (EVCA) wholeheartedly applauds today’s announcement by the Food and Drug Administration that it is putting the controversial tobacco “deeming” regulation on hold for five years as it looks to balance regulation and encouraging the development of innovative, less dangerous tobacco products.

The announcement came on the heels of a letter sent by Hartland, Wisconsin to the FDA yesterday (July 27) that the agency either begin coordination proceedings to align the federal “deeming” rule with local economic interests, or face a lawsuit. The letter included some 70 pages of evidence that the deeming rule would devastate a local vaping manufacturer and major economic driver.

“Today the FDA opened the door to coordination,” said Mark Block, EVCA founder and director. “What Commissioner (Scott) Gottlieb and Mitch Zeller laid out in their announcement today goes hand-in-hand with what Hartland demanded.”

The new FDA plan calls for delaying the timeline to submit product review applications for electronic nicotine delivery systems (ENDS) or e-cigarettes to Aug. 8, 2022. That time will allow the agency to develop public health standards and manufacturers to develop better, more complete applications. In addition, the FDA will actively work on gaining public input into its regulatory content.

“This is a total shift in agency policy from the bureaucratic “We will write it and you follow it” traditions at the agency,” Block said. “Hartland has insisted on public input starting with its third day of hearings back April. And pushing back the timeline for what would have been a very costly preapplication process shows the FDA clearly recognizes what Hartland has advised – it needs far more information from actual stakeholders before implementing such vague overreach.”

The July 27, 2017 letter to the FDA stated that coordination with Hartland can address and solve the following issues:

  • Online and television advertising of vapor products
  • Protecting youth from nicotine products
  • The burdens and costs of PMTA
  • The freeze on new products, innovation, and technologies
  • Labeling, Bottles, and Boxes
  • Warnings and accurate statements
  • Manufacturing standards
  • Online Sales
  • Excise taxes and flavor bans imposed by the states

“EVCA will continue to support coordination efforts in Hartland, and what will undoubtedly be more communities who can now see for themselves why the coordination process has been so successful in standing up to federal agencies,” said Block. “Until we see a complete overhaul of this regulation – such as legislation introduced by U.S. Rep. Duncan Hunter – there’s always threat the rule will destroy the vaping industry and smokers’ options to quit.”

 

Press Announcements > FDA announces comprehensive regulatory plan to shift trajectory of tobacco-related disease, death
Previous post

Coordination or lawsuit?

Next post

Why the Vaping Industry Should Utilize Litigation as a Deterrence (Part 1)

No Comment

Leave a reply

Your email address will not be published. Required fields are marked *