Search results for " automation"

Article Implications of Cell Culture Conditions on Protein Glycosylation
The authors present a review of the techniques commonly used for glycosylation analysis. By Michiel E. Ultee, PhD, Dr. Richard Easton This article reviews the implications of cell-culture co…

Article Biopharma Advances Demand Specialized Expertise
Jun 15, 2015 By BioPharm International Editors BioPharm International eBooks Volume 28, Issue 13 Contract service providers share insights on biopharma market developments and the impl…

Article Continuous Chromatography: Trends, Definitions and Approaches
When it comes to process control, it will be close to impossible to disagree with a statement that a continuous process will require more automation, more sensors, and thus will generate more data. On…

Article Detecting Protein Aggregates and Evaluating their Immunogenicity
Mar 01, 2015 By Randi Hernandez BioPharm International Volume 3, Issue 28 Aggregation in biopharmaceuticals remains a major concern and threatens the stability of a product. Protein …

Article Optimizing Resin Performance with Disposable Chromatography Solutions
From a technology perspective, there is the possibility to benefit from automation and also increased scale/size of batches produced. There have not been any major technical changes in the chromatogra…

Article Viral Clearance Challenges in Bioprocessing
Challenges remain for virus removal and validation. Nov 1, 2014 By: Cynthia Challener, PhD BioPharm International Volume 11, Issue 27, pp. 42-44 Removal and inactivation of adventitio…

Article DoE Provides Benefits, but Preparation Is Necessary
Nov 1, 2014 By: Cynthia Challener, PhD BioPharm International Volume 11, Issue 27, pp. 28-29  Using a design-of-experiment (DoE) approach allows a formulation development scientist t…

Article Challenges and Trends in Biopharma Facility Design
These advantages include further reduction in manufacturing footprint and [capital expenditures], in combination with an opportunity for more robust processing because there is a higher degree of auto…

Article Biopharma Moves to Integrated, Single-Use, Downstream Processing
… has been a lack of adequate technology, particularly in the sensor area, that provides for a robust automation approach, according to Pora. “Not all downstream process steps are available in single …

Article Challenges in Analytical Method Development and Validation
Experts give insight on method transfer, QbD, and regulations for analytical method development and validation for biopharmaceuticals. The manufacture of biopharmaceuticals presents …

Previous PageNext Page