The US Food and Drug Administration (FDA) has increased the amount of mandatory information required to report a problem with an e-cigarette device in order to “identify new or concerning trends” ...
Are you already a subscriber? login here
Are you already a subscriber? login here
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.