Authors
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Organizational Structures of Process Development and Manufacturing SupportHow to strike a balance between site autonomy and global coordination.
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Elevating Your Charge Variant and Aggregate Analysis for Biotherapeutic Proteins*Monday, March 22, 2021 at 9am EDT| 1pm GMT | 2pm CET, Monday, March 22, 2021 at 2pm EDT| 1pm CDT | 11am PDT* High resolution is one of the key challenges in modern biopharmaceutical analysis. In this webinar learn the importance of considering the entire liquid chromatography (LC) system to gain optimum results and maximum resolution from your LC column. *On demand available after final airing until March 22, 2022*
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Matching Tools to Biophysical Analysis DemandsMethod choice is crucial to when seeking answers to biosimilar characterization questions.
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Intensification of a Chromatography PlatformThe authors present a shift toward more integrated purification processes.
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Intensification of a Chromatography PlatformThe authors present a shift toward more integrated purification processes.
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Intensification of a Chromatography PlatformThe authors present a shift toward more integrated purification processes.
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Intensification of a Chromatography PlatformThe authors present a shift toward more integrated purification processes.
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Intensification of a Chromatography PlatformThe authors present a shift toward more integrated purification processes.
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Going from Fed-Batch to PerfusionPerfusion processes can attractive for biologics drug manufacturing; however, obstacles remain.
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Assessing Viral Inactivation for Continuous ProcessingTesting demonstrates an automated semi-continuous process strategy for viral inactivation with steps that mimic batch processing.
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STR Profiling: Authentication of Human Cell Lines and BeyondShort tandem repeat profiling is the most validated method to confirm cell line identity and avoid misidentified or cross-contaminated cell lines.
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STR Profiling: Authentication of Human Cell Lines and BeyondShort tandem repeat profiling is the most validated method to confirm cell line identity and avoid misidentified or cross-contaminated cell lines.
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Platform for Integrated Continuous BioprocessingContinuous processing of 100 g of monoclonal antibody in 24 hours has been demonstrated using lab-scale equipment.
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STR Profiling: Authentication of Human Cell Lines and BeyondShort tandem repeat profiling is the most validated method to confirm cell line identity and avoid misidentified or cross-contaminated cell lines.
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Addressing the Challenges in Downstream Processing Today and TomorrowNewer classes of biotherapies will require innovations in processing technology.
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Rapid Sterility Tests for Short Shelf-Life Products: A Risk-Based ApproachUSP experts share current perspectives on a risk-based approach to rapid sterility tests for short shelf-life products such as cell and gene therapies. Live: Wednesday, May 9, 2018 at 12 pm EDT | 11 am CDT | 9 am PDT / On Demand available after airing until May 9, 2019. Register free: http://www.biopharminternational.com/bp_w/rapid
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Implementing Single-Use Technology in Tangential Flow Filtration Systems in Clinical ManufacturingA case study evaluates the performance, control of operations, productivity, and cost savings of a single-use system.
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Analytical Strategy in the Development of BiosimilarsThe author outlines an analytical strategy for establishing similarity in biosimilar development and approval.
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Automated Concentration and Diafiltration of Multiple siRNA SamplesProject: transfer a manual concentration/diafiltration process for siRNA production.
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Standards and Best Practices to Support Trace Metal Quantitation in Cell Culture Chemically Defined Media and Hydrolysates–Review best practices for measurement of trace elements in cell culture media and hydrolysates, developed in a collaboration between USP and the BioPhorum Operations Group. Live: Tuesday, Mar. 3, 2020 at 11am EST | 8am PST | 4pm GMT | 5pm CET On demand available after airing until Mar. 3, 2021 Register free
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Using Simulation to Address Capacity LimitationsModeling tools help process engineers optimize a biopharmaceutical facility’s capacity.
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Using Simulation to Address Capacity LimitationsModeling tools help process engineers optimize a biopharmaceutical facility’s capacity.
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Using Simulation to Address Capacity LimitationsModeling tools help process engineers optimize a biopharmaceutical facility’s capacity.
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Using Simulation to Address Capacity LimitationsModeling tools help process engineers optimize a biopharmaceutical facility’s capacity.
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Using Simulation to Address Capacity LimitationsModeling tools help process engineers optimize a biopharmaceutical facility’s capacity.
