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Supporting evidence-based analysis for modified risk tobacco products through a toxicology data-sharing infrastructure
The US FDA defines modified risk tobacco products (MRTPs) as products that aim to reduce harm or the risk of tobacco-related disease associated with commercially marketed tobacco products. Establishing a product’s potential as an MRTP requires scientific substantiation including toxicity studies an...
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| Udgivet i: | F1000Res |
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| Main Authors: | , , , , , , , , , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
F1000Research
2017
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5657032/ https://ncbi.nlm.nih.gov/pubmed/29123642 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.12688/f1000research.10493.2 |
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