Proceedings of the Ninth International Conference of Drug Regulatory Authorities (ICDRA) - Berlin, Germany 25-29 April 1999
(1999; 102 pages) Voir le document au format PDF
Table des matières
Ouvrir ce répertoire et afficher son contenuOpening Ceremony
Ouvrir ce répertoire et afficher son contenuGood regulatory practice
Ouvrir ce répertoire et afficher son contenuGood certification practice
Ouvrir ce répertoire et afficher son contenuCounterfeit drugs: challenges and solutions
Ouvrir ce répertoire et afficher son contenuCurrent issues in regulation and quality
Ouvrir ce répertoire et afficher son contenuInternational Conference on Harmonization: implementation and implications
Ouvrir ce répertoire et afficher son contenuDrug utilization studies
Ouvrir ce répertoire et afficher son contenuInternational Conference on Harmonization and the common technical document
Ouvrir ce répertoire et afficher son contenuKeynote address
Fermer ce répertoireGlobal and national efforts to reduce tobacco use
Afficher le documentHow national authorities can promote non-smoking: experience from a European Union country
Afficher le documentInternational implications of the regulation of nicotine products
Afficher le documentPublic health responsibilities of nicotine regulation
Afficher le documentDiscussion
Afficher le documentRecommendations
Ouvrir ce répertoire et afficher son contenuElectronic communication in the regulatory process
Ouvrir ce répertoire et afficher son contenuTransparency in monitoring the safety of medicines
Ouvrir ce répertoire et afficher son contenuPharmaceutical products for use in special groups
Ouvrir ce répertoire et afficher son contenuNeed for Bioequivalence
Ouvrir ce répertoire et afficher son contenuAntimicrobial resistance: battling the bugs
Ouvrir ce répertoire et afficher son contenuSafety issues of plasma-derived medicinal products
Ouvrir ce répertoire et afficher son contenuHerbal medicines
Ouvrir ce répertoire et afficher son contenuRegulation and access to essential drugs
Afficher le documentParticipants
Afficher le documentBack cover
 

International implications of the regulation of nicotine products

Mr D. Sweanor, Canada

Of the various forms of nicotine-containing products, tobacco, the most harmful (dirtiest) nicotine delivery system, is the least regulated. Tobacco products are cheap, widely promoted and easy to get, whereas alternative nicotine preparations are subject to strict regulatory control as pharmaceutical products.

This has created the “nicotine maintenance monopoly” in which nicotine causes dependence and the delivery vehicle causes the disease and the existing regulatory system forces all who want or need nicotine on an ongoing basis to get it from tobacco products. The health toll is quite high, but the potential to reduce this health toll is also significant, as most of the 1.15 billion cigarette smokers want to quit, or otherwise reduce harm.

Thus, there is a huge potential market but the present legal environment does not allow ´clean’ alternatives to replace the ´dirty’ nicotine delivery system. Regulatory change would be required to promote greater access to nicotine dependence treatment products and a wider range of indicated uses of these products for smoking reduction, temporary abstinence and longer-term substitution.

Only then will tobacco companies lose the ´nicotine maintenance monopoly’. To this end, drug regulators should enter into dialogue with nicotine experts, tobacco control experts and pharmaceutical companies.

vers la section précédente vers la section suivante
 

Dernière mise à jour: le 3 mai 2013