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Postmarketing Surveillance for “Modified-Risk” Tobacco Products
INTRODUCTION: The U.S. Food and Drug Administration (FDA) acquired authority to regulate tobacco products in 2009. This authority will provide a structured process for manufacturers to introduce products that may have “modified-risk” for morbidity or mortality relative to traditional tobacco product...
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2012
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| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3242968/ https://ncbi.nlm.nih.gov/pubmed/21330282 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/ntr/ntq243 |
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