Search results for " sterile"
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				Validation of the Production of Influenza Virus
								
	This application note describes the validation of the single-use ReadyToProcess WAVE 25 rocking bioreactor system in production of influenza virus from Vero cells in microcarrier-based cultures. A 2…								
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				Evaluating E&L Studies for Single-Use Systems
								Small-scale assembly extraction study 
		
		
			The small-scale assembly option was applied to a fill/finish manufacturing process that involved the use of a single-use polyethylene mixing bag, steril…								
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				Drug Quality Key to Innovation and Access
								These challenges apply to biosimilars and cutting-edge therapies, as well as to the need for modern aseptic processing methods able to reliably produce both new and generic sterile injectables. The in…								
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				Advancing Single-Use Technology Through Collaboration
								
	By working together to harmonize the highly variable steps within the biopharmaceutical manufacturing process, both end users and suppliers are making strides toward the efficiency and integrity of …								
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				Designing a Biomanufacturing Facility Incorporating Single-Use Technologies
								
	Asking the right questions is crucial to establishing a facility design. 
	By Peter Genest, John Joseph 
	The benefits of adopting single-use technologies in the production of biopharmaceuticals…								
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				Selecting the Right Viral Clearance Technology
								
	By Cynthia Challener, PhD 
	The introduction of adventitious viral agents is a recognized, inherent risk of biologic drug production that is well addressed by international regulatory requirements…								
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				Using Single-Use Technologies in Downstream Processing
								According to Nilesh Mehta, senior process engineer, Merck GTO, Sterile and Validation COE, “as new technologies become available or existing technologies are converted into a single-use format, the nu…								
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				Quality Systems Key to Lifecycle Drug Management
								
	Jun 01, 2015 
	
	By Jill Wechsler 
	
	BioPharm International 
	
	Volume 28, Issue 6 
	The submission and review of manufacturing supplements is costly and time consuming for biopharmaceutical comp…								
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				Modular Manufacturing Platforms for Biologics
								
	May 01, 2015 
	
	By Randi Hernandez 
	
	BioPharm International 
	
	Volume 28, Issue 5 
	It should come as no surprise that the good design principles governing the execution of pharmaceutical manu…								
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				Continuous Chromatography: Trends, Definitions and Approaches
								I have also heard comments that continuous operation requires sterile columns, which lends itself to the notion that the columns need to be disposable. Obviously, prevention of bioreactor contaminatio…