Search results for " IND" in Articles / App Notes
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				Scaling Up Novel Therapies
								Within the past decade, however, the industry has achieved significant improvement by adopting technologies that allow more predictable outcomes, says Alex Chatel, product manager at Univercells. Bior…								
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				FDA Seeks to Enhance Manufacturing of Cell and Gene Therapies
								Clinical development is crucial, but industry needs to have “manufacturing under control,” Marks observed. 
	
	More support
	
		FDA’s Regenerative Medicine Advanced Therapy (RMAT) program can help exp…								
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				Understanding Validation and Technical Transfer, Part 3
								 This third article in a three-part series (1,2) dealing with validation and technical transfer in the biopharmaceutical industry discusses validation of a non-traditional biopharmaceutical process, l…								
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				Transformative Medicines Challenge FDA and Manufacturers
								FDA reports that some 40 companies are developing CAR-T technologies for multiple indications and that it is monitoring more than 600 active investigational new drug applications (INDs) related to gen…								
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				Continuous Processing for the Production of Biopharmaceuticals
								By Anurag Rathore, Nikhil Kateja, Harshit Agarwal, Abhishek Kumar Sharma 
	Benefits of continuous processing have been widely demonstrated by a variety of manufacturing industries. With the growing …								
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				Viral Clearance Challenges in Bioprocessing
								Processes with fewer purification steps present a challenge to virus clearance, however, because higher removal claims are expected with individual unit operations. “Access to high titer virus prepara…								
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				HT Multi-Product Liquid Chromatography for Characterization of Monoclonal Antibodies
								Monoclonal antibodies (MAbs) are an important class of therapeutic proteins in biotechnology and have been developed to treat a variety of indications to fill significant unmet medical needs.1 MAbs ge…