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Exploring the Food and Drug Administration’s review and approval of Entresto (sacubitril/valsartan)
Federal regulatory agencies such as the United States Food and Drug Administration review pharmacological evidence to ensure the safety and efficacy of new and repurposed pharmaceuticals prior to market approval. The discussions, disagreements and procedural decisions contained within such reviews o...
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| Pubblicato in: | Pharmacol Res Perspect |
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| Autori principali: | , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
John Wiley and Sons Inc.
2021
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8177063/ https://ncbi.nlm.nih.gov/pubmed/34087050 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/prp2.794 |
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