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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....
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| Main Authors: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
MDPI
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4085595/ https://ncbi.nlm.nih.gov/pubmed/24732068 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/pharmaceutics6020195 |
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