Search results for "biopharm" in Articles / App Notes
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				Selecting a Comprehensive Bioburden Reduction Plan
								Targeting Bioburden 
	
	BioPharm: What type of planning is necessary to target all aspects of bioburden reduction? 
	Mittelman and Anicetti (PDA task force): The most important consideration in biob…								
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				Re-use of Protein A Resin: Fouling and Economics
								Bracewell 
	
	BioPharm International 
	
	Volume 3, Issue 28 
	In the past two decades, Protein A affinity chromatography has remained the de facto capture step for purification of monoclonal antibod…								
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				Impurity Testing of Biologic Drug Products
								Method development and validation
			
				BioPharm: What is the right approach to method development and validation for therapeutic proteins? 
			
			
				Kang (Patheon): Two concepts are key to appro…								
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				Modular Manufacturing Platforms for Biologics
								…d by applying methods described in Federal Standard 209 may affect operations of a cleanroom” for biopharmaceutical processes. Thus, the company writes, a measure of both viable and nonviable particl…								
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				Detecting Protein Aggregates and Evaluating their Immunogenicity
								Particle-detection methods 
	
	There are various detection technologies that should be used to address protein aggregation needs at various phases of the biopharmaceutical development process; however…								
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				Tackling Analytical Method Development for ADCs
								“Cross-fertilization within the biopharmaceutical industry, particularly driven by the proliferation of ADC-focused conferences, workshops, instrument company webinars, etc., has lead to an increased …								
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				Trends in BioPharma Approvals in 2013
								A total of 16 approvals were recorded in Europe, while only six biopharmaceuticals came on the market in the US in that same period. This trend can partly be explained by Europe playing catch up in th…								
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				Milestones and Moderate Progress in 2012 Drug Approvals
								Twelve biopharmaceutical marketing applications were approved in the United States and/or the European Union in 2012 (see Table I). Approval numbers for the past year are in line with those recorded o…								
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				Addressing the Challenges in Downstream Processing Today and Tomorrow
								While there is agreement on the value of process and product understanding, there is often debate within most biopharmaceutical companies on the extent of QbD investment and underlying cost implicatio…								
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				Moving Biosimilars Forward in a Hesitant Market
								On the pricing pressure aspect in the biopharma market, Gabrielson asserts that pricing pressure is a central theme in biosimilars. “That is why these products exist, fundamentally,” he remarks, “to m…