Search results for " report" in Articles / App Notes
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				The Evolving Role of Starting Materials in Cell and Gene Therapy
								The Alliance for Regenerative Medicine reports that as of the end of 2018, 263 cellular therapies and 362 gene-modified cellular therapies were being evaluated in clinical trials (see Figure 1) (4). T…								
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				Emerging Therapies Test Existing Bioanalytical Methods
								Bone marrow transplants, a similar form of treatment, have become relatively common since the initial reported use in 1968. 
	Gene therapy, the transfer of genetic material into specific cells to mo…								
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				What’s New in Upstream Technologies
								The company also reports that it supplies process buffers at a fraction of the resources and facility space, resulting in a more streamlined buffer suite and a more efficient manufacturing process. Th…								
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				Biomanufacturing: The Cost of Unskilled Workers
								First, a 2018 report from BioPlan Associates estimates there are well over 10,000 therapeutics in R&D, both drugs (chemical substance pharmaceuticals) and biopharmaceuticals (biotechnology-derived pha…								
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				State of the Biopharmaceutical Industry: Lessons from 2018 Survey Data
								The results, published in the Annual Report and Survey of Biopharmaceutical Manufacturing Capacity and Production, provide a detailed, data-rich look at current trends in the biopharmaceutical industr…								
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				Understanding Validation and Technical Transfer, Part 3
								Initially, development information can be kept in research or laboratory notebooks, but as clinical use becomes likely, formal development reports and initial validation work should be prepared, revie…								
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				Making the Move to Continuous Chromatography
								There needs to be a way to analyze and report these data seamlessly, as well as detect adverse trends in performance,” she explains.  
	
	
		Regulatory aspects are the second area of concern. Here, Le…								
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				Preclinical Evaluation of Product Related Impurities and Variants
								In addition, it has been reported that GCSF has a free cysteine residue (cys-17) that can trigger aggregate formation, and so post-manufacturing aggregation of GCSF is a possibility (13). Recombinant …								
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				Ensuring Sterility in Small-Scale Production
								…as defined in FDA’s aseptic processing guidance (1), the Parenteral Drug Association’s Technical Report #62 (2) on manual aseptic processing, and in EudraLex Volume 4, Annex 1 (3). In other words, th…								
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				Biopharma in 2016: Higher Quality Drugs, Less Expensive Manufacturing
								According to Cytiva, the cost of a KUBio plant can be as much as 45% lower than a comparable, traditional facility 
	
	This year, Process Development Forum will continue to report on drug approvals, i…