Availability, accessibility, usage and regulatory environment for novel and emerging tobacco, nicotine or related products
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The European Commission Health and Consumer Directorate-General (DG SANCO) commissioned RAND Europe, by way of the Executive Agency for Health and Consumers, in the framework of the Health Programme (No SC 2010 6306), to examine the availability, accessibility, usage and regulatory environment for novel and emerging tobacco, nicotine and related products in European Union Member States. Drawing on a range of methodological approaches involving systematic evidence review, key informant interviews with representatives from industry, including retailers, and a survey of stakeholders at national governmental and non-governmental agencies, this report will serve to inform further a possible revision of the Tobacco Products Directive 2001/37/EC. The report also provides an up-to-date overview of the evidence and basis for current tobacco and related products regulation that may be of interest to a wider audience interested in tobacco control policies.
Table of Contents
Availability, accessibility and use of novel and emerging tobacco, nicotine or related products: evidence review
Marketing of novel and emerging tobacco, nicotine or related products: key informant interviews
Availability, accessibility and use of novel and emerging tobacco, nicotine or related products: stakeholder survey
Evidence review stage I
Key informant interview topic guide
Abbreviated survey addressed to medicines agencies
Regulation of novel tobacco and nicotine products by type of regulation
Research conducted by
The research described in this report was prepared for the Executive Agency for Health and Consumers (EAHC) and conducted by RAND Europe.
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