Search results for " preparative"
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				Getting a Handle on Biopharma’s Most Critical Quality Attributes and Quality Control
								
	While the multiple attributes method gains ground and traditional lab methods improve, broad efforts are underway to determine biopharmaceuticals’ most significant critical quality attributes and en…								
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				Single-Use for Downstream Chromatography: Benefit or Hindrance?
								
	Single-use technology is gaining ground in downstream bioprocessing, but challenges stall further adoption.
	By Feliza Mirasol
	
	
	
	ARTMOIS/STOCK.ADOBE.COM
	
	Biopharmaceutical manufactu…								
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				What’s New in Upstream Technologies
								
	Recent upstream processing innovations include enhanced sensor technology, single-use bioreactors, and automated cell culture systems. 
	
	
	
	By Amber Lowry  
	
	
	
	
	SCIENCE PHOTO - STOCK.A…								
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				Cytiva Opens Biotechnology Manufacturing Center in UK
								GE Healthcare Opens Biotechnology Manufacturing Center in UK
	
		Cytiva is opening a biotechnology manufacturing center at the Stevenage Bioscience Catalyst (SBC) Open Innovation Campus, in Stevenage…								
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				Using Multiple Techniques in Biosimilar Analysis
								
	Application of multiple techniques at different conditions presents a more complete picture of a dynamic situation.
	By Rebecca Strawn 
	
	
	
	
	Sergey/stock.adobe.com
	Almost all drug product…								
								 					Resource
				
				PREP Symposium
								PREP 2019 is the longest running, most recognized international scientific conference and exposition driving the field of Preparative and Process Chromatography, organized by expert scientists and eng…								
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				Understanding Validation and Technical Transfer, Part 3
								Understanding Validation and Technical Transfer, Part 3
	Validation ensures safe and effective biologic products that benefit the patients whose health and wellbeing depend on the therapies. Part 1 |…								
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				Putting Viral Clearance Capabilities to the Test
								
	Process understanding and careful assessment of risks are essential in developing viral clearance programs. 
	
	  
	
	By Rita C. Peters 
	
	  
	
	 
	nobeastsofierce/Shutterstock.com 
	
	
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				Freedom to Roam During Protein Purification Runs
								
	Have you ever felt tied to your ÄKTA system and itching to get out of the lab? Consider this scenario: You have started a run in the lab and want to get some work done in your office. You may …								
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				Industry Adoption of Single-Use Systems Remains Low
								
	Single-use technologies are starting to gain ground as capacity needs change, but industrywide adoption remains low. 
	
	  
	
		
			
				
				
				  
			
			
				By Feliza Mirasol 
			
			
				zli…