Cell And Gene Therapy Manufacturing
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Innovative Contamination Control: Enabling Integrity And Efficiency
10/15/2024
An integrated approach can enhance contamination control, boost process efficiency, and ensure the production of high-quality cell therapy products.
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Collaborating with the FDA: Dr. Peter Marks and Dr. Nicole Verdun Share Advice For Small And Emerging Biotechs
1/30/2024
In this segment, Dr. Peter Marks and Dr. Nicole Verdun share their advice and best practices for small and emerging biotechs when working with the FDA.
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Interview With Pharma Analytics Field Application Specialist - Sandi True
11/6/2025
Hear Sandi True, a Field Applications Specialist discuss helping customers navigate challenges often encountered when evaluating and implementing Residual DNA Quantitation, Mycoplasma Detection, and Microbial Identification Assays.
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Manufacturing Considerations For Viral & Non-Viral Platform Selection
6/24/2025
In this webinar, a panel of experts spanning the lentiviral vector, exosome and oncolytic virus fields will discuss the impact of manufacturing considerations on their respective platform selection and ongoing product/process development strategies.
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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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Simplify Your Process Of Choosing An Optimal Resin
5/19/2025
Discover how to address evolving biotherapeutic purification challenges with a diverse resin portfolio and an intuitive Resin Selection Tool designed to streamline workflows and enhance production efficiency.
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Thermo Fisher Scientific Bio-Expo Live 2024: Downstream Bioprocessing
8/15/2024
Review downstream process tools from Thermo Fisher Scientific to enable optimal biologics purification, including chromatography resins, chemicals, process liquids, and buffers.
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Knowledge Culture: Downstream Innovation
6/2/2025
In this workshop, you’ll learn about various solutions, from cell isolation to cell expansion, that can support autologous and allogeneic cell therapy process needs, digital automation, and mycoplasma testing.
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Defining The CMC / Clinical Relationship For Allogeneic Cell Therapies
5/6/2024
During this segment, Nguyen and Wagner define why the relationship between CMC and Clinical is so critical, and they also explain what a mutually beneficial partnership between CMC and Clinical looks like.
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Mitigating Risk In Process Automation
8/18/2023
Two Chief Technical Officer's for therapeutic organizations cover the various ways in which automation helps to reduce risk and why closing systems and reducing the number of manual manipulations is so critical.