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Consumer advice and details of how to report problems with e-cigarettes with guidance on how to place an e-cigarette on the market in Great Britain and Northern Ireland, including the notification scheme.
Advice for Retailers and Producers
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
There is an obligation on the manufacturers and importers of electronic cigarettes to submit a notification of such products they intend to market.
UK government interpretation of the requirements for labelling e-liquids for Great Britain
Healthcare professionals should be vigilant for suspected adverse reactions and safety concerns associated with e-cigarettes and e-liquids, commonly known as vapes. Please report adverse reactions to the Yellow Card scheme and promote vigilance among patients.
UK government interpretation of the requirements for labelling e-liquids for Northern Ireland.
If you put EEE on the UK market you must follow rules on both the EEE you sell and the EEE that becomes waste (WEEE).
General advice on vigilance - electronic cigarettes devices and refill containers.
Submission of notifications for Northern Ireland under article 20 of directive 2014/40/EU.
Advice on ingredients in nicotine-containing liquids in electronic cigarettes and refill containers.
Dose of nicotine delivered & uptake and consistency of dose.
Register a new manufacturer's mark and access lists of approved and inactive measuring container bottles (MCB) marks.
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