Cell And Gene Therapy Manufacturing
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Thermo Fisher Scientific Suzhou, China Manufacturing Site Capabilities
11/2/2018
Watch this video to learn more about this manufacturing site capabilities, quality management systems, PPI implementation, product expansion, assurance of supply and lead times.
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Simple In-House Mycoplasma Testing Method For Regulatory Expectations And Rapid, Confident, And Actionable Results
5/29/2025
In this webinar, we present an overview of worldwide regulatory guidance for mycoplasma testing, as well as a mycoplasma testing method that has been accepted by regulatory authorities worldwide across various therapeutic modalities.
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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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CTS DynaCellect Fluidics Demonstration
6/9/2025
Streamline and customize your cell processing workflow with automated, precise control over fluid movement and transfer parameters.
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Breaking Down Automated Manufacturing
8/18/2023
Experts explain the general benefits of automated manufacturing as well as the key areas that need improvement to scale up quality and to help reduce the costs of therapeutics.
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BioTitan Retention Device Overview
5/29/2025
Learn about a retention device that provides robust fortification for single-use assemblies. Its 360-degree seal strengthens connections, reduces leak risks, and ensures process integrity for fluid transfer.
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Accelerating Process Scale-Up From Benchtop To Commercialization- From Controller To Software
11/4/2025
Discover strategies for optimizing process control, refining media selection, and ensuring safety through rigorous contaminant detection to mitigate development risks.
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Innovations In Mycoplasma And Sterility Testing For Biopharma
5/22/2025
In this webinar, our expert speakers will discuss the types of analytical testing that can be effectively employed in the early stages of therapeutic development and subsequently scaled to meet production challenges.
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Market Demand For AAV Vectors
11/13/2023
Here, Dave Maheu, VP, Head of Process & Analytical Development at Candel Therapeutics and Curran Simpson, Chief Operating Officer at REGENXBIO detail the key factors driving the adeno associated virus manufacturing market.
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Analytical Approaches For Quantifying Residual Host Cell DNA
5/29/2025
In this webinar, we’ll discuss the challenges, risks and considerations involved in developing and using in-house residual testing solutions, and the benefits of using commercial kits for residual DNA testing.