As a long time customer of White Cloud (long before I became a Customer Service Sentinel for the company) I have had the pleasure of using every product we have brought to market over the last 5 years. While my mainstay is the ClearDraw and […]
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FDA Vaping Regulations vs. Vaping Advocacy
The vaping industry has endured its fair share of controversies over the last few years. From bad science and scare-mongering news headlines to strict laws placing vaping under the same category as smoking, it’s no wonder why vapers have felt the need to step up […]
Continue ReadingFDA Vaping Regulations: Importing and Exporting
When it comes to the FDA’s regulation of vaping products, there have been concerns with how the rules affect the importing and exporting of products in and out of the US. With the history of the FDA’s involvement in the vaping industry dating back to […]
Continue ReadingFDA Vaping Regulations: Vape Shops
One of the biggest concerns regarding the FDA’s regulation of vapor products is the impact it will have on small vape shops. Most vape shops are privately owned, family-run businesses – what you might call “mom-and-pop shops”. Many of these smaller vapor product retailers built […]
Continue ReadingFDA Vaping Regulations: E-Liquids & Nicotine
When it comes to e-liquids and nicotine, the requirements listed in the FDA’s regulations for vaping products have created a bit of confusion – especially when it comes to nicotine-free e-liquids. The FDA has listed out regulations for both nicotine-containing and nicotine-free e-liquids and has […]
Continue ReadingFDA Vaping Regulations: The DIY Market
Although the FDA’s Deeming Regulations are contained within an extensive 499-page document, some areas of regulation were left a bit hazy. Among the haze is how the regulations affect the DIY vaping market, or more specifically how the rules will affect the individual components that […]
Continue ReadingFDA Vaping Regulations: Substantial Equivalence
Among the 499 pages of the FDA’s Deeming Regulations is an option to avoid the PMTA process if a manufacturer can prove that any of their products introduced to the market after the set grandfather date of February 15, 2007, are “substantially equivalent” to a […]
Continue ReadingFDA Vaping Regulations: The Grandfather Date
One of the most controversial stipulations included in the FDA’s Deeming Regulations is the grandfather date, which was set with the passing of the Tobacco Control Act of 2009. The grandfather date exempts tobacco products from the premarket tobacco application process if they were on […]
Continue ReadingFDA Vaping Regulations: Premarket Tobacco Applications
Now that the FDA has authority to regulate vapor products as tobacco products, all vapor products that entered the market after the set grandfather date of February 15, 2007, are required to enter the FDA’s regulatory approval process to remain on the market. This process […]
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