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Emergency use authorization of medicines: History and ethical dilemma
The regulatory approval process of the United States Food and Drug Administration and European Union is the most demanding and challenging worldwide. They have the provision of the expedited approval pathways, i.e., “Emergency use authorizations” and “Conditional marketing authorizations,” respectiv...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Wolters Kluwer - Medknow
2023
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10267997/ https://www.ncbi.nlm.nih.gov/pubmed/37325578 http://dx.doi.org/10.4103/picr.picr_149_22 |