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Young patients’ involvement in a composite endpoint method development on acceptability for paediatric oral dosage forms

BACKGROUND: In line with the European Paediatric Regulation, the European Medicines Agency (EMA) asks for investigation of a medicine’s acceptability in paediatric medicines development. A standardised acceptability testing method combining the outcome of “swallowability” and “palatability” assessme...

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Detalles Bibliográficos
Autores principales:	Reidemeister, Sibylle, Nafria Escalera, Begonya, Marín, Daniel, Balayla, Jan, Klingmann, Ingrid, Klingmann, Viviane
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2023
Materias:	Methodology
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10688476/ https://www.ncbi.nlm.nih.gov/pubmed/38031172 http://dx.doi.org/10.1186/s40900-023-00520-8

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