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Analytical Challenges and Regulatory Requirements for Nasal Drug Products in Europe and the U.S.
Nasal drug delivery can be assessed by a variety of means and regulatory agencies, e.g., the Food and Drug Administration (FDA) and the European Medicines Agency (EMA) have published a set of guidelines and regulations proposing in vitro test methods for the characterization of nasal drug products....
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
MDPI
2014
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4085595/ https://www.ncbi.nlm.nih.gov/pubmed/24732068 http://dx.doi.org/10.3390/pharmaceutics6020195 |