Thermo Fisher Webinars
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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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Digital Design Meets Proven Performance: The Future Of Single-Use Assemblies
3/31/2026
Single-use assembly design is evolving fast. Learn how scalable platforms, digital automation tools, and global supply networks are converging to support sustainable biopharma manufacturing at scale.
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Achieving High Purity In Complex Antibody Formats
7/29/2025
Discover innovative purification strategies and workflow designs for next-generation antibody formats and learn to overcome challenges in achieving high purity and yield.
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Supporting Development Of mRNA Therapeutics By Enabling Commercial-Scale mRNA Purification
6/9/2025
Discover the next generation of scalable affinity capture for high-quality mRNA purification. Learn how a simple, reliable binding mechanism can maximize efficiency and simplify your manufacturing process.
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Enhancing Protein Quality Through Optimized Galactosylation
7/23/2025
Advance your understanding of critical protein engineering. Explore expert strategies for optimizing complex molecular structures, paving the way for more effective and consistent biological products.
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Leveraging Rapid Sterility Testing To Advance Cell Therapy Production
6/23/2025
Explore the crucial role of rapid sterility testing in cell therapy manufacturing. This presentation delves into the benefits of swift, accurate detection for product quality and patient safety.
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Quality Roundtable: Raw Material Planning For Tech Transfer And Scaling Biologics
1/22/2025
Join this roundtable of biopharmaceutical professionals as they share their insights to help you navigate important quality and planning decisions for the progression of your biologic.
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Manufacturing Friendly Aggregate Clearance In Downstream Processing
5/19/2025
In this webinar, results are shared from the evaluation and preliminary optimization of a mixed-mode chromatography unit operation designed for aggregate removal in flow-through mode using a high-throughput POROS resin with immobilized caprylic acid.
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Reducing Particulate-Related Batch Risk In Bioprocessing
7/1/2026
Increasing scrutiny around particulate contamination is pushing teams to act earlier. Understanding where risks originate and applying proactive strategies can ease challenges across production.
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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.