Search results for " safety" in Articles / App Notes
								 					Article
				
				Advances in Sterilization Technologies for Overcoming Viral-Vector Manufacturing Challenges
								…al and overarching, and adherence to strict quality standards is essential to ensure consistency and safety for patients.
	Scaling considerations
	
	Scaling itself does not necessarily increase the…								
								 					Article
				
				Gene Therapies Push Viral Vector Production
								“For lentiviral packaging, there are iterative cycles of safety improvements. Agilent vectors, for example, are suitable and compatible with generation-four packaging systems (i.e., the latest version…								
								 					Article
				
				An Analytical Approach to Biosimilar Drug Development
								By Feliza Mirasol 
	
	
	  
	The long-term safety and efficacy of biosimilars are largely based on clinical studies that have already been conducted on the reference biologic, but these studies may…								
								 					Article
				
				Evaluating E&L Studies for Single-Use Systems
								Regulatory guidelines require that the product contact items “shall not be reactive, additive, or absorptive” to assure drug product quality and safety (2). The manufacturer is, therefore, responsible…								
								 					Article
				
				Regulation of Biosimilars: A Matter of Variability, Similarity, and Comparability
								…eutical or reference product to which biopharmaceuticals will have to show comparability in quality, safety, and efficacy to be approved as biosimilars. 
	
	
		Revised guidelines on general principle…								
								 					Article
				
				Quality by Design: A CMO's Perspective on Gaining Knowledge Faster and Better
								QTPP is defined in ICH Q8 (R2) as "a prospective summary of the quality characteristics of a drug product that ideally will be achieved to ensure the desired quality, taking into account safety and ef…								
								 					Article
				
				Putting Viral Clearance Capabilities to the Test
								Bergmann, manager, viral safety and clearance services, Eurofins Lancaster Laboratories. “The key parameters that determine the scope of the study are the clinical stage and indication of the product …								
								 					Article
				
				Evaluating Surface Cleanliness Using a Risk-Based Approach
								Cleaning in the GMP industry is a critical process intended to prevent or, in more modern terms, reduce risk of contaminating the subsequent product with undesirable residues that may impact patient s…								
								 					Article
				
				Innovative Therapies Require Modern Manufacturing Systems
								Most of its $132 million budget increase goes to expanding food safety programs, but small amounts are allotted to ensuring the accuracy of genetic tests important to precision medicine, expanding for…								
								 					Article
				
				The Bullish Outlook for Biosimilars
								… approved and implemented stricter regulatory guidelines that put a greater emphasis on efficacy and safety (6). 
	
	
	In contrast to these other markets, the United States has surprisingly been a la…