Cargando...
Power of the Dissolution Test in Distinguishing a Change in Dosage Form Critical Quality Attributes
For a dissolution method to be considered relevant to in vivo performance, the dissolution data profiles should show discrimination or meaningful change when there is a change in critical material attributes (CMAs) and critical product properties (CPPs). The dissolution test has been shown repeatedl...
Gardado en:
| Publicado en: | AAPS PharmSciTech |
|---|---|
| Autor Principal: | |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Springer International Publishing
2018
|
| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6848239/ https://ncbi.nlm.nih.gov/pubmed/30350251 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1208/s12249-018-1197-7 |
| Tags: |
Engadir etiqueta
Sen Etiquetas, Sexa o primeiro en etiquetar este rexistro!
|