Cell And Gene Therapy Manufacturing
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                    Nunc Standard Closed Cell Factory System
                        2/2/2022
                    
This clean and closed system is designed to provide consistent and high-quality results to enhance your adherent cell culture processes. This ready-to-use system will help you quickly develop and scale up your processes with standard components for supply assurance.
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                    Advancing The Purification Of VSV-G Pseudotyped Lentiviral Vector
                        6/9/2025
                    
Discover new strategies to overcome lentiviral purification challenges with a scalable approach that maintains viral infectivity through gentle processing conditions.
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                    Perfusion: Planning A Run
                        6/16/2025
                    
Learn about a logical approach for defining the operation of a perfusion run. We will break down the process using the three following steps: knowledge space, design space, and control space.
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                    Master The 2-Point Calibration Process  To Maintain Data Integrity
                        5/19/2025
                    
Ensure accurate sensor readings with an innovative software by mastering the 2-point calibration process. Learn more about how and why regular calibration supports data integrity and compliance.
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                    A Robust, Future-Ready Solution That Adapts To Your Needs
                        5/22/2025
                    
Explore a future-ready solution that features advanced automation, intuitive design, and scalable solutions to streamline your bioprocessing workflows and prepare your operations for future growth.
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                    Solutions For Diverse Biomolecule Purification
                        5/21/2025
                    
Interview with Paul Lynch, Product Management Leader, Purification, discusses our chromatography resins and innovations in downstream purification processes.
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                    CMC Comparability: Transitioning to Commercial Manufacturing with Dr. Nicole Verdun
                        1/30/2024
                    
In this segment, Dr. Nicole Verdun shares some of the challenges demonstrating CMC comparability during late-stage product development (i.e., pivotal or Phase 3 clinical trial) that occur while transitioning to commercial manufacturing.
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                    Why Clinical Requirements Change: Dr. Peter Marks on Pre-IND Meeting Pathways 
                        1/30/2024
                    
Learn how clinical requirements change after the FDA and a company agree on a pathway during a pre-IND meeting and how the company might recover as a result.
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                    Accelerating Bioprocessing Success With Analytics
                        5/19/2025
                    
This bioprocessing online webinar series talks about analytical solutions to help accelerate bioprocessing success. There are a variety of analytical options available to help you gain deeper insights on your cell culture process.
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                    Knowledge Culture Basics — Gene Therapy Education Series: Lentiviral Vectors
                        6/9/2025
                    
In this session of our ongoing education series on lentiviral vectors, we delve further into principles of lentiviral transduction and challenges in suspension-based lentivirus production.