Search results for " impurities"
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				How to develop a scalable rAAV process
								
	
	
	Adeno-associated virus (AAV) is the most common vector for gene therapy, yet there’s much room to improve production, purification, and analytics. Here we present the latest updates to our wor…								
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				From cells to purified capsids: How to develop a scalable rAAV process
								
	
	
	
	Adeno-associated virus (AAV) is the most common vector for gene therapy, yet there’s much room to improve production, purification, and analytics. In this webinar we present the latest upd…								
								 					Webcast
				
				Controlling Cell-Culture Process Variability
								Impurities in raw materials are a risk to your cell productivity and protein quality. That is why we created a transparent, multi-source supplier network for cell-culture materials.								
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				Virus and exosome purification: harness core bead technology
								
	
	
	
	Using core bead technology to fine tune impurity removal and maximize recovery of 
	
	large entities.
	
	
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				Analytical Considerations for Successful Upstream Process Development with Spivey and Lane
								If you have an upstream process that is generating material that has too many impurities or too much variation in the glycosylation pattern, then folks are going to say, “I can't clean this up with ch…								
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				Insider Recommendations for Getting Started with Mechanistic Modeling of Chromatography
								And the good news is that you are able to do this, not only for your molecule of interest, but also for all the impurities. 
	
	
		Nick, how do you do this in reality? 
	
	
		Whitelock: Absolutely. So…								
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				Setting Up Bioprocessing Systems for Digital Transformation
								
	Digitalization of bioprocessing operations, equipment, and facilities can improve workflow and output, but maintaining data integrity is a concern. 
	By Feliza Mirasol 
	The advancement of digit…								
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				Manage HCPs and Enhance Your Route to Market
								
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	Host cell protein (HCP) management is critical to biologics development—and getting it wrong could delay your development cycle. Learn how the right HCP strategy can enhance…								
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				The Importance of Process Intensification and PAT for Achieving Real-Time Release
								
	
		
			
				Creativity and collaboration are required to overcome complex method development challenges. 
				
				  
			
			
				
				
				  
			
			
				By Kelvin H. Lee and Mark Lies 
			
			
			…								
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				Virus-like Particles as Therapeutic Moieties of the Future
								In addition, various non-desired impurities such as media components, debris, host DNA or RNA, and exosomes may be retained in the final product (14). Modification of VLPs may also affect their downst…