Académique Documents
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MEDICAL JOURNAL
Vol 118 No 1213 ISSN 1175 8716
The Ministry of Health has recently started a process for enhancing tobacco product
regulation, and has invited public submissions to this Review. 1 While this is a very
positive development, it is part of a pattern of narrowly focusing on particular tobacco
control interventions—smokefree policies, marketing restrictions, tobacco taxation,
media campaigns, and cessation. 2,3 Little thought has been given to the overall policy,
regulatory, and organisational framework in which these interventions might occur.
This article suggests a new approach to the regulation of tobacco in New Zealand.
The current Review provides us with an opportunity to consider the setting in which
new labelling, disclosure, and product control regulations might be most effective.
Given that reducing tobacco-related harm is one of the most important means of
improving health status and reducing health inequalities in New Zealand,4 the
suitability of the regulatory framework and organisations for tobacco control is a
significant health sector issue. There is the potential to prevent thousands of cases per
year of unnecessary premature death and disability amongst New Zealanders. A
disproportionate number of these cases are amongst Maori, Pacific peoples, and low-
income New Zealanders.
Tobacco control in New Zealand has had some effect in reducing smoking prevalence
and raising awareness of the associated health issues. However, since 1991, there has
been little change in overall smoking prevalence, and little improvement for Maori or
the most disadvantaged.
The problem of an insufficiently regulated industry
The importance of the current Review can be seen by the present situation, where
neither the government nor the public know what is in particular tobacco products,
how the products are constructed, or what the consequences are of any design change.
Nor do they have any mechanism for finding much of this information. Government
In 2001, the World Health Assembly of the World Health Organization (WHO)
passed a resolution that recognised the subversive nature of the tobacco industry. The
Assembly expressed ‘great concern [about] the findings of the Committee of Experts
on Tobacco Industry Documents, namely, that the tobacco industry has operated for
years with the expressed intention of subverting the role of governments and of WHO
in implementing public health policies to combat the tobacco epidemic’.17 The
Committee of Experts on Tobacco Industry Documents reported in July 2000 that the
attempted subversion had been ‘elaborate, well financed, sophisticated, and usually
invisible’.18
A possible model: marketing control
We suggest that the regulatory frameworks suggested by Borland 19 and Liberman20
are required for the effective regulation of tobacco. These frameworks would enable
the Government to make tobacco companies only sell products in New Zealand to a
Tobacco Authority, would give government the ability to specify the constituents in
the products, and could remove the ability of companies to sell branded products to
retailers or customers. Essentially, such frameworks place a non-profit organisation
between tobacco manufacturers and retailers, removing the profit motive from the
marketing of tobacco to consumers (but not from retailing). We suggest that, to cover
any costs to Government, the costs of such an Authority be fully recovered by a levy
on the suppliers of tobacco to the Authority.
Such an authority would have at least five ways of reducing or removing tobacco-
related harm. They are: modifying tobacco products; changing the way that the
products are marketed; offering substitutes (e.g. nicotine replacement therapy);