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...

Descripción completa

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

Internet

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

Ejemplares similares