Integrated Process Modeling—A Process Validation Life Cycle Companion

During the regulatory requested process validation of pharmaceutical manufacturing processes, companies aim to identify, control, and continuously monitor process variation and its impact on critical quality attributes (CQAs) of the final product. It is difficult to directly connect the impact of si...

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Detalles Bibliográficos
Autores principales: Zahel, Thomas, Hauer, Stefan, Mueller, Eric M., Murphy, Patrick, Abad, Sandra, Vasilieva, Elena, Maurer, Daniel, Brocard, Cécile, Reinisch, Daniela, Sagmeister, Patrick, Herwig, Christoph
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5746753/
https://www.ncbi.nlm.nih.gov/pubmed/29039771
http://dx.doi.org/10.3390/bioengineering4040086

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5746753/
https://www.ncbi.nlm.nih.gov/pubmed/29039771
http://dx.doi.org/10.3390/bioengineering4040086

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