Search results for " biopharms" in Articles / App Notes
								 					Article
				
				Selecting a Comprehensive Bioburden Reduction Plan
								
	Process maps and risk assessments are among the valuable tools operators can apply to reduce the risk of microbial contamination. 
	By Randi Hernandez 
	There are multiple variables to consider …								
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				Re-use of Protein A Resin: Fouling and Economics
								
	Mar 01, 2015 
	
	By Anurag S. Rathore, Mili Pathak, Guijun Ma, Daniel G. Bracewell 
	
	BioPharm International 
	
	Volume 3, Issue 28 
	In the past two decades, Protein A affinity chromatography ha…								
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				Impurity Testing of Biologic Drug Products
								
	Experts share insights on the various methods used for purity and impurity analysis of therapeutic proteins. 
	
	  
	
		
			
				By Adeline Siew, PhD  
			
		
		
			
				CA-SSIS/shutterstock.comIm…								
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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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				Detecting Protein Aggregates and Evaluating their Immunogenicity
								
	Mar 01, 2015 
	
	By Randi Hernandez 
	
	BioPharm International 
	
	Volume 3, Issue 28 
	Aggregation in biopharmaceuticals remains a major concern and threatens the stability of a product. Protein …								
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				Tackling Analytical Method Development for ADCs
								
	Feb 01, 2015 
	
	By Cynthia Challener, PhD 
	
	BioPharm International 
	
	Volume 28, Issue 2 
	The targeted therapy possible with antibody-drug conjugates (ADCs) makes them an attractive class of …								
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				Trends in BioPharma Approvals in 2013
								In 2013,  20 products containing new biopharmaceutical molecular entities (defined herein as recombinant proteins, monoclonal antibody or biosynthesized nucleic acid-based products) were approved in t…								
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				Milestones and Moderate Progress in 2012 Drug Approvals
								
	 
	
	   
First gene therapy and plant-based expression vector products approved in 2012. 
	
	In terms of product approvals, the past year can be considered reasonably successful. Twelve biopharm…								
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				Addressing the Challenges in Downstream Processing Today and Tomorrow
								
	Newer classes of biotherapies will require innovations in processing technology. 
	By Glen R. Bolton, Bernard N. Violand, Richard S. Wright, Shujun Sun, Khurram M. Sunasara, Kathleen Watson, Johna…								
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				Moving Biosimilars Forward in a Hesitant Market
								
	
	
	The biosimilars landscape is growing as market factors, such as pricing pressure, advanced bioprocessing and analytical technologies, and upcoming patent expirations for innovator biologics dr…