AbstractA model based approach has been developed and used to identify robust operating conditions for an industrial hydrophobic interaction chromatography where resin lot variability, combined with feed stream variability, was resulting in serious performance issues during the purification of a multi component therapeutic protein from crude feed material. An equilibrium dispersive model was formulated which successfully predicted the key product critical quality attribute during validation studies. The model was then used to identify operating parameter ranges that assured product quality despite the process variability. Probabilistic design spaces were generated using stochastic simulations that showed the probability that each resin lot ...
Downstream processing in the manufacturing biopharmaceutical industry is a multistep process separat...
As defined by ICH [1] and FDA, Quality by Design (QbD) stands for “a systematic approach to developm...
Increased product yield at reduced cost and time has been the driving force of any manufacturing pro...
AbstractA model based approach has been developed and used to identify robust operating conditions f...
One of the major issues in the pharmaceutical industry today is the cost of development and validati...
This paper presents a model-based method to aid in the process validation for the purification of ph...
To design efficient and safe biopharmaceutical production processes, understanding the process and h...
Process development, optimisation and robustness analysis for chromatography separations are often e...
This work presents a methodology for analyzing and optimizing preparative chromatographic processes....
AbstractThe development and validation of a chromatography rate model for an industrial multicompone...
Process development, optimization and robustness analysis for chromatographic separation are often e...
The separation of one weakly and one strongly binding impurity from a therapeutic protein by ion-exc...
In the production of pharmaceutical drugs, a large part of the production costs stem from the downst...
A dream of many pharmaceutical companies is to be able to register a large design space with the reg...
Model-based process design is increasingly popular when designing pharmaceutical purification proces...
Downstream processing in the manufacturing biopharmaceutical industry is a multistep process separat...
As defined by ICH [1] and FDA, Quality by Design (QbD) stands for “a systematic approach to developm...
Increased product yield at reduced cost and time has been the driving force of any manufacturing pro...
AbstractA model based approach has been developed and used to identify robust operating conditions f...
One of the major issues in the pharmaceutical industry today is the cost of development and validati...
This paper presents a model-based method to aid in the process validation for the purification of ph...
To design efficient and safe biopharmaceutical production processes, understanding the process and h...
Process development, optimisation and robustness analysis for chromatography separations are often e...
This work presents a methodology for analyzing and optimizing preparative chromatographic processes....
AbstractThe development and validation of a chromatography rate model for an industrial multicompone...
Process development, optimization and robustness analysis for chromatographic separation are often e...
The separation of one weakly and one strongly binding impurity from a therapeutic protein by ion-exc...
In the production of pharmaceutical drugs, a large part of the production costs stem from the downst...
A dream of many pharmaceutical companies is to be able to register a large design space with the reg...
Model-based process design is increasingly popular when designing pharmaceutical purification proces...
Downstream processing in the manufacturing biopharmaceutical industry is a multistep process separat...
As defined by ICH [1] and FDA, Quality by Design (QbD) stands for “a systematic approach to developm...
Increased product yield at reduced cost and time has been the driving force of any manufacturing pro...