Search results for " GMP"
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Innovations in Cell Culture: Manufacturing the Future
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“Innovations in Cell Culture” is a new virtual series from Cytiva, where we will explore and discuss the needs of the biopharma industry with a panel of industry …
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How To Execute Successful Data Migrations
Successful migrations require careful planning to meet business needs and maintain data integrity.
By Art Meisler
Data migration is the unglamorous task of a system implementation. …
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Technology Innovations Improve Process Chromatography Performance
“We are also seeing that, as regulatory limits impose restrictions for ensuring customer safety, like toxicology and cleaning validation for GMP [good manufacturing practices] environments, off-the-sh…
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Tapas & TECH Talks: Panel Discussion with Cytiva/IQVIA
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When developing a new therapy, it is more important than ever to have the future in mind from the outset. The choices you make at each step can set you up for …
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Next Generation Process Chromatography
Hardick: With HiTrap™ Fibro PrismA now launched for R&D applications, the teams are working hard to ensure this is followed soon by the launch of the GMP units capable of purifying up to 15-kg mAb in …
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Gene Therapies Push Viral Vector Production
“We must bring robust, scalable, industrialized manufacturing processes as fast as possible (less manual and more automated processes) and GMP solutions for both small-scale and large-scale production…
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Cytiva Expands Offering for ReadyToProcess™ Columns
You can enjoy the flexibility of using our prepacked ReadyToProcess columns from benchtop to full-scale manufacturing in GMP environments.
Explore ReadyToProcess columns
List of columns here
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Maximizing the Effectiveness of Upstream Bioprocessing Through the Combination of Lab Informatics and Instrumentation
By establishing effective management of data and knowledge, it will be possible to employ advances, such as artificial intelligence and synthetic biology, to their full potential in upstream bioproc…
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Tips for Viral Vector Production
In this blog article, insights are shared around the challenges in viral vector manufacturing and how to achieve a scalable and cost-efficient process suitable for GMP manufacturing environments.
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Monitoring and Control of Inline Dilution Processes
We also developed an operator control platform that is flexible and familiar to GMP [good manufacturing practice] production environments,” Gach remarks.
The company has also incorporated buffer…