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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Detalles Bibliográficos
Autores principales: Trows, Sabrina, Wuchner, Klaus, Spycher, Rene, Steckel, Hartwig
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2014
Materias:
Review
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

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4085595/
https://www.ncbi.nlm.nih.gov/pubmed/24732068
http://dx.doi.org/10.3390/pharmaceutics6020195

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