General
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Guidance on the Tobacco Products Directive
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Facilitate transition to regulatory compliance
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Report European regulatory developments
Strategy
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Advise on regulatory strategy for UK and other european markets (Country-Specific Information)
Notifications
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Prepare, submit and co-ordinate Notifications across Europe
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Liaise with the relevant regulatory body to facilitate processing of Notifications
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Advise on the Classification, Labelling and Packaging of Chemicals (CLP Regulation 1272/2008)
Manufacturing Operations
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Advise on best practice for the manufacture of e-cigarettes and e-liquids (EU Manufacturing Standard)
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Write and maintain technical dossiers
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Advise on best practice for packaging and labelling
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Conduct raw material internal supplier audit
Vigilance
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Provide guidance on establishing a Vigilance system
Sample analysis at Analytical Laboratory
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Test e-liquid (heated and unheated) for nicotine concentration and contaminants
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Test devices for consistent dosing and emitted contaminants
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Arrange shelf life testing on e-liquids and devices
Toxicological Assessment
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Generate relevant toxicological data for Notifications
Product Development
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Advise on best practice for development of new products and improve existing ones