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The new FDA e-cigarette regulations require the manufacturer to make the case that their product ‘presents less risk than other tobacco products’ among other things. In the absence of a predicate tobacco product, the case is made in a Premarket Tobacco Product Application (‘PMTA’). But for a range of e-liquids, for example, how much does a PMTA...
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On the morning of the 24th June we woke up to the news that – after 43 years of union – the United Kingdom had voted to leave the European Union. By a narrow margin the Vote Leave campaign had won and a ‘Brexit’ is underway. These are uncertain times and unchartered waters as no...
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The nicotine concentration claim on the label of an e-liquid should be accurate i.e. the label claim should match the actual nicotine content or as close as reasonably possible. But what should be the acceptable limit – or tolerance – of actual nicotine concentration? Should it be  +/- 5%, 10% or 15% of label claim?  More?   E-liquid Manufacturing...
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On 16th November 2015 a new milestone in the e-cigarette world was reached: the first electronic cigarette was licensed as a medical product. But it never made it to market. We wrote about the product back in 2015 – and now, with the recent announcement by Public Health England, we take a refresh look at the...