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Analysis of FDA’s IQOS marketing authorisation and its policy impacts
BACKGROUND: Philip Morris Products SA (PMPSA) submitted a premarket tobacco application (PMTA) to US Food and Drug Administration (FDA) seeking an order permitting it to market IQOS in the USA. US law requires FDA to deny marketing authorisation if applicants fail to demonstrate that their product i...
Gardado en:
| Publicado en: | Tob Control |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
2020
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7952009/ https://ncbi.nlm.nih.gov/pubmed/32601147 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/tobaccocontrol-2019-055585 |
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