Search results for " packaging" in Articles / App Notes
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				Understanding Validation and Technical Transfer, Part I
								…visions, authorized FDA to issue good manufacturing practice (GMP) regulations for “manufacturing, packaging, or holding of finished pharmaceuticals.” Those regulations were finalized in 1963 as 21 C…								
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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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				Bioburden Control in the Biopharmaceutical Industry
								  
	
	
		 
		
	
	
		The basic standards for establishing a facility for manufacturing, processing, and packaging biopharmaceutical products should, therefore, ensure that these three criteria are met …								
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				Best Practices for Data Integrity
								
	
		Best Practices for Data Integrity
		
			Optimize practices and meet requirements using electronic data integrity systems. 
		
		
			
				By Jennifer Markarian 
			
			
				
			
			
				Maintainin…								
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				The New World of Biopharmaceutical Manufacturing
								
	Industry experts discuss the single-use revolution and changes to upstream and downstream processing equipment. 
	
	  
	
		
			
				
			
			
				By Jennifer Markarian 
				
			
			
				
			
		
		
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				Single-use Bioreactors Have Reached the Big Time
								“For example, Pall’s SU bioreactors come with special packaging and an easy-to-implement biocontainer installation method that eliminate the main causes of integrity failures,” she says. 
	Suppliers…								
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				Evaluating E&L Studies for Single-Use Systems
								
	Extraction studies demonstrate approaches for evaluating single-use bio-pharmaceutical manufacturing materials. 
	By Irene Cecchini, Daniele Mastroianni, Silvia Rocchi, Gabriella Angiuoni 
	Biop…								
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				Drug Quality Key to Innovation and Access
								
	FDA plans to advance initiatives for ensuring reliable production of drugs and biologics in 2017. 
	By Jill Wechsler 
	Amidst multiple challenges to the structure and governance of the US health…								
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				The Tide Stays High
								…s that cater to clinical development (clinical supplies manufacturing, analytical services, clinical packaging, and clinical research). Many CDMOs have told PharmSource that they are operating near c…								
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				Innovation vs. Capacity: How CMOs Compete
								
	The strategies of an innovation-driven CMO may be different than a capacity-driven CMO. 
	By Jim Miller 
	While industry participants and observers talk about the “CMO industry,” they know that …