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There is an obligation on the manufacturers and importers of electronic cigarettes to submit a notification of such products they intend to market.
Advice on names and presentation of nicotine-containing electronic cigarettes and refill containers on packaging.
Advice on submitting annual reports for electronic cigarettes and refill containers. Submission of notifications under part 6 of the tobacco and related products regulations 2016.
General advice on due diligence - electronic cigarettes devices and refill containers.
For manufacturers reporting adverse incidents with joint replacement implants under the vigilance system.
For manufacturers reporting adverse incidents with intraocular lenses under the vigilance system.
Submission of notifications for Northern Ireland under article 20 of directive 2014/40/EU.
Guidance for healthcare establishments that manufacture medical devices in-house.
For manufacturers reporting adverse incidents with biological/mechanical surgical heart valves under the vigilance system.
General advice on vigilance - electronic cigarettes devices and refill containers.
Poster with advice for healthcare professionals on how to carry out point of care testing safely and correctly.
Submitting notifications on the European common entry gate. Submission of notifications for Northern Ireland under article 20 of directive 2014/40/EU.
Submission of notifications for northern Ireland under article 20 of directive 2014/40/EU.
Advice on submitting annual reports for electronic cigarettes and refill containers.
For manufacturers reporting adverse incidents with neurostimulators under the vigilance system.
Advice on ingredients in nicotine-containing liquids in electronic cigarettes and refill containers.
Dose of nicotine delivered & uptake and consistency of dose.
UK government interpretation of the requirements for labelling e-liquids for Northern Ireland.
Don’t include personal or financial information like your National Insurance number or credit card details.
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