Search results for "analytical"
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				Essentials in Quality Risk Management
								…hase during drug development and manufacturing and changes in drug-product formulation, definition, analytical method, and associated process changes are understood and managed to ensure patient safe…								
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				The Importance of Partnering for Bioanalytical Studies
								By Feliza Mirasol
	
	
		Bioanalytical studies are an important aspect in biologic drug development because data from these studies are needed to define the characteristics of potential new biologic …								
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				Maximizing the Effectiveness of Upstream Bioprocessing Through the Combination of Lab Informatics and Instrumentation
								Advances in analytical instruments are one key part of the solution. Novel techniques including Raman spectroscopy and other advanced monitoring methods have the potential to reduce the reliance on di…								
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				Methods Accelerate Biosimilar Analysis
								In May 2019, FDA published a draft guidance on the analytical assessment and other quality-related considerations for biosimilars, clarifying regulatory requirements and expectations for demonstration…								
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				Evaluating E&L Studies for Single-Use Systems
								Analytical methods 
		
		
			In the three case studies, the following analytics were applied: 
		
		
			• Headspace sampling/gas chromatography/mass spectrometry (HS/GC/MS) and gas chromatography/mass…								
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				A Platform Approach for the Identity Testing of Multi-Component Cell-Culture Media
								The developed testing algorithm, which incorporates a combination of few relatively simple analytical methods such as osmolality, quantitation of glucose, and folic acid, provides specific identity co…								
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				Virus-like Particles as Therapeutic Moieties of the Future
								In this 44th article in the “Elements of Biopharmaceutical Production” series, the authors review the status of VLPs as therapeutics as well as challenges associated with their analytical and function…								
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				Managing Residual Impurities During Downstream Processing
								Increased understanding of potential impurities and their consequence to the ultimate quality, safety, and efficacy of biopharmaceuticals--as well as improvements in analytical technology that provide…								
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				Witnessing Major Growth in Next-Generation Antibodies
								Additional analytical and regulatory demands 
	Next-generation antibodies also have their own set of analytical and regulatory challenges. With respect to analytical methods, each format/target comb…								
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				Improving PAT for Biologics
								Dec 01, 2014 
	
	By Cynthia Challener, PhD 
	
	BioPharm International 
	
	A key component of the quality-by-design (QbD) approach to pharmaceutical manufacturing is the implementation of process ana…