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Vaccines After an Emergency Use Authorization (EUA): Modern Evidence Generation Approaches
Every medical product requires additional study even after regulatory approval. We highlight several lines of enquiry to advance our understanding of COVID19 vaccines post authorization: identifying key population segments warranting more study, assessment of efficacy, and of safety data, harmonizat...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Springer International Publishing
2021
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8061154/ https://www.ncbi.nlm.nih.gov/pubmed/33886112 http://dx.doi.org/10.1007/s43441-021-00290-z |