Search results for "biopharma 4.0"
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				Applying GMPs to the BioPharma Supply Chain
								
	Defining best biopharmaceutical practices is necessary to ensure the safety of the supply chain. 
	Manufacturing biopharmaceuticals carries great responsibility. The drugs produced must be availab…								
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				Trends in BioPharma Approvals in 2013
								In 2013,  20 products containing new biopharmaceutical molecular entities (defined herein as recombinant proteins, monoclonal antibody or biosynthesized nucleic acid-based products) were approved in t…								
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				A Look Ahead at BioPharma Manufacturing and Regulation
								
	 
	
	   
The FDA talks about the changing scope of regulatory science. 
	 
	
	   
	
		Regulatory science underpins innovation and practices in drug manufacturing. The most common definition of r…								
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				Getting a Handle on Biopharma’s Most Critical Quality Attributes and Quality Control
								
	While the multiple attributes method gains ground and traditional lab methods improve, broad efforts are underway to determine biopharmaceuticals’ most significant critical quality attributes and en…								
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				The Value of Digital in Biopharma
								
	To be successful in making targeted therapies, biopharma manufacturing must evolve into smaller, faster, and more efficient environments. Digital technology and data science can be leveraged to add …								
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				The Pulse on the Industry - BioPlan and the Biopharma Resilience Index
								
	 
	
	This podcast is an informative and accessible discussion on the biopharma industry’s needs and possible solutions being taken to address these issues. 
	LISTEN TO THE PODCAST >  
								
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				Fluid Handling in Biopharma Facilities
								
	Industry experts discuss challenges, trends, and innovations in fluid handling.
	By Susan Haigney
	Contamination prevention in biopharmaceutical manufacturing is crucial, and the proper handling…								
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				Continued Process Verification for Biopharma Manufacturing
								
	The authors discuss complications of implementing continued process verification and provide recommended approaches. 
	Oct 1, 2014 
	
	By: Jeff Fleming, Robin Payne 
	
	BioPharm International 
	
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				Emerging biopharma: progressing a biologic drug to market
								
	
	
	  
	
	
	
	There are many pitfalls in the road to developing and bringing a new therapy to market. Understanding some of these areas and being prepared to make the right decisions at the right ti…								
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				A Stepwise Approach to a Digital Transformation in Biopharma
								
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An interview on “smart” manufacturing—a paradigm shift towards digital transformation for improved safety and quality, optimized performance, and increased complianc…