Search results for " GMP" in Articles / App Notes
Article
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…
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Addressing the Complex Nature of Downstream Processing with QbD
These risk assessments are influenced by platform data, previous process characterization knowledge, available GMP data, and subject matter expertise. DoE activities are applied where appropriate mode…
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Moving PAT from Concept to Reality
In the near future, Sartorius Stedim Biotech also expects wider spread adoption of analytics in GMP that are already available, such as spectroscopy for metabolite control and bio-capacitance for viab…
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Ensuring Viral Safety of Viral Vaccines and Vectors
Density separation using ultracentrifugation is possible but is challenging at GMP manufacturing scale.
Conclusion
Viral contamination of vaccines, albeit rare, can lead to serious human healt…