Search results for " outsource" in Articles / App Notes
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				What's in Your SOP?
								They are many virtual and small companies that outsource much of their operations. US 21 Code of Federal Regulations (CFR) 200.10 discusses the relationship between a contract provider and a contract …								
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				Biopharma Advances Demand Specialized Expertise
								
	Jun 15, 2015 
	
	By BioPharm International Editors 
	
	BioPharm International eBooks 
	
	Volume 28, Issue 13 
Contract service providers share insights on biopharma market developments and the impl…								
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				Buffer Management Solutions for Large-Scale Biomanufacturing
								
	Learn how different approaches can resolve buffer management challenges in large-scale biomanufacturing. This article discusses solutions such as inline conditioning, outsourcing buffer preparation,…								
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				Automation Trend in Fill/Finish Reduces Contamination Risk
								
	Aseptic fill/finish is crucial in biopharma manufacturing and is optimized through automated technology.
	
	
	By Feliza Mirasol 
	
	
	
	Aseptic filling is a crucial process in biopharmaceutical …								
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				Being Thorough When Transferring Technology
								
	Communication and taking the time to develop the process are key to successful transfer and scale up of biologics. 
	By Susan Haigney 
	Editor's note: The following is an extended version of the…								
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				Aseptic Processing: Keeping it Safe
								
	By Randi Hernandez, BioPharm International 
	
	
	Humans represent the greatest risk for microbial contamination in an aseptic process. 
	
	Aseptic processing has garnered some increased scrutiny…								
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				Drug Discovery and Development in India
								
	Apr 01, 2015 
	
	By Jane Wan 
	
	BioPharm International 
	
	Volume 28, Issue 4 
	Indian pharmaceutical companies’ entry into the drug discovery and development field dates back to the early 1990s …								
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				Advancing QbD in the EU
								In a discussion paper issued in late 2012, the agency pinpointed the need for tighter controls on outsourced manufacturing to ensure that it is GMP compliant. EMA also thought that details of the "pre…								
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				Discovering the unknown: How does in silico process development change PD scientists’ work?
								As resources are sometimes limited, an alternative strategy that is taken by some customers is actually to outsource modeling activities to Cytiva and to use the expertise that we have here at Cytiva …								
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				Developing oligonucleotide therapeutics with confidence
								
	
	
	
In this video, we will look at key considerations for oligo therapeutic developers entering the market, such as scalability, flexibility, regulatory concerns, insource/outsource consideratio…