With the advent of EU regs and most certainly upcoming FDA regs on ecig under the hammer of tobacco products (and as medical devices downstream - not if but when), I wonder how manufacturers are approaching this event? Are manufacturers hopeful they will go away (0), concerned but with a specific direction forward to address regulatory requirements (1), worried as hell because of additional costs to business and vapers with little knowledge of FDA compliance (2), or scared s***less and in possible danger of extinction (3)?
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