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Article Insights and Strategies for Successful Development of Scalable AAV Processes: Part 2 of 2
part2 Click here to view more Industry Leader Q&As >> In the second of a two-part series, Anki Magnusson, Staff Research Engineer, Protein and Viral Production, and Åsa Hagner…

Article Top Challenges to Overcome When Developing AAV Processes: Part 1 of 2
AAVprocessdevelopment Click here to view more Industry Leader Q&As >>  In the first of a two-part series, Anki Magnusson, Staff Research Engineer, Protein and Viral Producti…

Article How to Optimize and Scale Up AAV Production
In this article from a roundtable discussion, four experts from academia and industry met to discuss challenges in refining and scaling up AAV production pipelines to meet the increasing demand for …

Article Efficient Sodium Hydroxide Sanitization with a Novel Procedure of AxiChrom™ Columns Packed with Chromatography Resin
Here, we describe a microbial challenge test with a concentration of 1-M NaOH to mimic typical sanitization practices employed by the biopharma industry for a broad range of resins. The final version …

Article Virtual Scientific Symposium: Process Development: Go Smarter, Go Faster!
There, you can hear from industry leaders, visit our exhibition booth, and ask our panelists questions. 

Article Genetic Vaccine Platforms Demonstrate Their Potential
“The knowledge level for some of the required production techniques, such as the formulation of lipid nanoparticles, is still limited within the pharmaceutical industry. We can expect to accrue even m…

Article High-Quality Chromatography System Meets Predesigned DeltaV for Integrated Manufacturing
Implementing a distributed control system for facility-wide control of biomanufacturing can help overcome these issues by supporting the industry with improved data management and quality control.

Multimedia Cell Culture Media Considerations and Optimization for Improved Titers and Protein Quality
Peggy Lio, Senior Director of Global Cell Culture Services at Cytiva, explores the evolution of bioprocessing over the last 30 years, parameters to consider when developing cell culture media, and wha…

Article Updating Viral Clearance for New Biologic Modalities
“The industry has a way to go in developing a range of viral clearance products that enable efficient separation of more complex mAbs, such as bispecific or Fc-fusion proteins,” he says. Another c…

Article Single-Use Technologies Are Here to Stay: How Can We Improve Their Supply?
Click here to read more >> The use of single-use technologies has been growing steadily, but supply constraint is a key challenge for the biopharma industry. This article discusses the potenti…

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