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Kurt Brorson

Showing results (31-40 of 67) with videos related to

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International Journal of Pharmaceutics|August 31, 2016
A design space exploration for control of Critical Quality Attributes of mAbHemlata Bhatia, Erik Read, Cyrus Agarabi, et al.
Biotechnology Progress|September 4, 2009
Salt tolerant membrane adsorbers for robust impurity clearanceWilliam T Riordan, Steven M Heilmann, Kurt Brorson, et al.
Biotechnology and Bioengineering|May 22, 2019
Validation and optimization of viral clearance in a downstream continuous chromatography settingMeng-Jung Chiang, Mark Pagkaliwangan, Scott Lute, et al.
Journal of Pharmaceutical Sciences|August 25, 2020
High Performance Size Exclusion Chromatography and High-Throughput Dynamic Light Scattering as Orthogonal Methods to Screen for Aggregation and Stability of Monoclonal Antibody Drug ProductsAshwinkumar Bhirde, Bhaskara Vijaya Chikkaveeraiah, Ramesh Venna, et al.
PDA Journal of Pharmaceutical Science and Technology|February 8, 2014
Role of risk assessments in viral safety: an FDA perspectiveLixin Xu, Sang Bong Lee, Chana Fuchs, et al.
Analytical Chemistry|October 17, 2019
Multi-Attribute Method for Quality Control of Therapeutic ProteinsSarah Rogstad, Haoheng Yan, Xiaoshi Wang, et al.
Journal of Industrial Microbiology & Biotechnology|February 7, 2013
Evidence for grow-through penetration of 0.2-μm-pore-size filters by Serratia marcescens and Brevundimonas diminutaSimran Kaushal, Brandi Gervais, Scott Lute, et al.
Biotechnology Progress|May 20, 2009
Removal of endogenous retrovirus-like particles from CHO-cell derived products using Q sepharose fast flow chromatographyDaniel M Strauss, Scott Lute, Kurt Brorson, et al.
Biotechnology Progress|April 1, 2015
Development of a modular virus clearance package for anion exchange chromatography operated in weak partitioning modeTimothy Iskra, Ashley Sacramo, Chris Gallo, et al.
PDA Journal of Pharmaceutical Science and Technology|February 2, 2012
Risk mitigation strategies for viral contamination of biotechnology products: consideration of best practicesAmy S Rosenberg, Barry Cherney, Kurt Brorson, et al.
Pageof 7

Showing results (31-40 of 67) with videos related to

Sort By:
Pageof 7
International Journal of Pharmaceutics|August 31, 2016
A design space exploration for control of Critical Quality Attributes of mAbHemlata Bhatia, Erik Read, Cyrus Agarabi, et al.
Biotechnology Progress|September 4, 2009
Salt tolerant membrane adsorbers for robust impurity clearanceWilliam T Riordan, Steven M Heilmann, Kurt Brorson, et al.
Biotechnology and Bioengineering|May 22, 2019
Validation and optimization of viral clearance in a downstream continuous chromatography settingMeng-Jung Chiang, Mark Pagkaliwangan, Scott Lute, et al.
Journal of Pharmaceutical Sciences|August 25, 2020
High Performance Size Exclusion Chromatography and High-Throughput Dynamic Light Scattering as Orthogonal Methods to Screen for Aggregation and Stability of Monoclonal Antibody Drug ProductsAshwinkumar Bhirde, Bhaskara Vijaya Chikkaveeraiah, Ramesh Venna, et al.
PDA Journal of Pharmaceutical Science and Technology|February 8, 2014
Role of risk assessments in viral safety: an FDA perspectiveLixin Xu, Sang Bong Lee, Chana Fuchs, et al.
Analytical Chemistry|October 17, 2019
Multi-Attribute Method for Quality Control of Therapeutic ProteinsSarah Rogstad, Haoheng Yan, Xiaoshi Wang, et al.
Journal of Industrial Microbiology & Biotechnology|February 7, 2013
Evidence for grow-through penetration of 0.2-μm-pore-size filters by Serratia marcescens and Brevundimonas diminutaSimran Kaushal, Brandi Gervais, Scott Lute, et al.
Biotechnology Progress|May 20, 2009
Removal of endogenous retrovirus-like particles from CHO-cell derived products using Q sepharose fast flow chromatographyDaniel M Strauss, Scott Lute, Kurt Brorson, et al.
Biotechnology Progress|April 1, 2015
Development of a modular virus clearance package for anion exchange chromatography operated in weak partitioning modeTimothy Iskra, Ashley Sacramo, Chris Gallo, et al.
PDA Journal of Pharmaceutical Science and Technology|February 2, 2012
Risk mitigation strategies for viral contamination of biotechnology products: consideration of best practicesAmy S Rosenberg, Barry Cherney, Kurt Brorson, et al.
Pageof 7