Advertisements which highlight the differences between e-cigarettes and tobacco may be more effective at promoting e-cigs than those which play up their similarities, a new study suggests.
The U.S. Food and Drug Administration (FDA) is to hold a workshop on battery safety to learn more about the risks of malfunctions in e-cig power sources and how to prevent them.
A manufacturer has argued that recent court statements by the U.S. Food and Drug Administration (FDA) show the agency does not have the authority to regulate vaping products that use synthetic nicotine. But will legislators and the courts agree?
U.S. media are buzzing with speculation that Donald Trump once again could be thinking outside the box as he seeks a reform-minded nominee to head the Food and Drug Administration, which recently extended its authority over e-cigarettes.
The U.S. Food and Drug Administration (FDA) has given a last-minute extension to some manufacturers of vapour products, allowing them an extra six months to register their companies and products as required by the deeming regulations.
Swedish Match has at last obtained some answers from the U.S. Food and Drug Administration (FDA) on its attempt to have snus products classified as modified risk – and they mix outright rejections with some very mild encouragement.
A drop in youth vaping has been recorded for the first time by a national U.S. survey, just days after the country’s surgeon general issued a high-profile report warning that use of e-cigarettes by young people was a dangerous phenomenon.
U.S. surgeon general Vivek Murthy has been accused of taking an inappropriate and unhelpful stance on vaping in his report “E-cigarette use among youth and young adults”.
U.S. Surgeon General Vivek Murthy’s report on the use of e-cigarettes by young people has drawn both criticism and praise. Representatives of the industry claimed the report ignored the benefits e-cigarettes can provide to those trying to avoid cigarettes, while medical groups and other organisations praised it and its call for action.
U.S. vape shop customers prefer to use tank-devices with flavours other than tobacco, and choose to buy these products from specialists because of their expertise and knowledge, according to a new study.
Philip Morris International (PMI) this week submitted its iQOS technology for approval as a reduced-risk product by the U.S. Food and Drug Administration (FDA), a strategy which if successful would provide a tremendous boost to the credibility of heat-not-burn and perhaps pave the way for PMI’s partner Altria to dominate that market in the United States.
While menthol as a flavouring for cigarettes comes under increasing attack, researchers consider its use – and that of other flavours – in the e-cigarette market.
Indiana law-makers have promised to replace the state’s controversial e-liquid manufacturing law during the next legislative session. The law specifies security requirements for e-liquid makers which most have not been able to achieve. The Republican party, which holds the majority in the Indiana state senate, has promised to address the law during the next session at its official Organization Day held on 22nd » Continue Reading.
Donald Trump has nominated Georgia Congressman Tom Price, a former orthopaedic surgeon, to become U.S. health secretary, in charge of future regulation of e-cigarettes.
Industry experts, regulators, lawyers and researchers will consider the implications of a complex picture of e-cigarette regulation when they meet at a conference in Washington next week.
Countries that ban vapour products could be breaking world trade agreements by unfairly privileging combustibles at the expense of e-cigarettes, two lawyers have warned.
Canada’s government today made its long-awaited move to end regulatory confusion with a new bill which puts vapour products in a category of their own, distinct from conventional tobacco.
Public vaping bans run contrary to best science and may have negative effects on public health, undermining efforts to combat smoking, according to a report by several leading academics.
An attempt to change the grandfather date in the FDA’s deeming regulations will not be taken up in the current lame-duck session of the U.S. Congress, a key law-maker in that effort said Thursday.
A federal judge in California has said that e-cig products only have to comply with FDA rules on labelling, and that state law can’t impose more rigorous requirements.
While many in the U.S. e-cigarette world hope that the Cole-Bishop proposal to change the FDA’s grandfathering date could be the industry’s salvation, at least one commentator believes it should be abandoned in the light of Donald Trump’s election to the presidency.
Sign up to access our business and regulatory briefings and get the most updated news, insights and our expert analysis to keep you on top of worldwide industry trends.
By signing up you agree to our Terms and Conditions Please note trial access may take up to 24 hours to be granted as access must be qualified by a member of the ECigIntelligence team.