WEBINARS AND VIDEOS

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DynaDrive S.U.B. Video Series

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DynaDrive Single-Use Bioreactors Drilled-Hole Sparge Technology

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DynaDrive Single-Use Bioreactors - One Reactor, Many Volumes

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Scale With Confidence From Bench To Commercial Production

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Why Is The Bioreactor Square? The Geometry Behind Exceptional Mixing

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Aegis Film For DynaDrive Single-Use Bioreactors

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Applying AI And Rapid Prototyping To Media And Process Development

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Five Reasons To Choose Thermo Scientific DynaDrive Single-Use Bioreactors

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Go Beyond Custom Media Screening And Prototyping

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Take The Lead With The Gibco CHOvantage™ GS Cell Line Development Kit

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Introducing The Applied Biosystems Resdnaseq Quantitative DNA System

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Efficient-Pro Medium And Feed Marketing

• Practical Solutions For Protein Analytics And Residual DNA Testing

  Discover practical solutions for common quality control bottlenecks in biotherapy manufacturing. Learn how to improve protein analytics and DNA testing robustness and accelerate time to market.

• Enabling Assurance Of Supply Through Evolving Bioprocessing Needs

  This featured event at the Gibco cell culture media 60th-anniversary in Grand Island, New York spotlights proactive strategies used by Thermo Fisher Scientific to decrease risk, ensure quality and meet customers raw material needs worldwide.

• HyPerforma DS 300 Single-Use Mixer Overview

  Watch this video to learn more about the Thermo Scientific HyPerforma Single-Use Mixer DS 300. This Modular mixing system offers a cost-effective, docking station-style mixing platform with multiple mixing-volume options.

• A Straightforward Path Toward Regulatory Compliance & Data Integrity With Your Microbial Testing Systems

  In this webinar, we will share a variety of strategies for implementing and validating microbial identification systems in the cGMP environment, possible difficulties along the way, and a comprehensive solution that addresses these challenges.

• Driving Sustainability In Bioprocessing With Biobased Single-Use Solutions

  Discover how biobased materials in bioprocessing enable measurable carbon emission reductions. Learn practical strategies to meet decarbonization goals and adopt greener, operationally sound practices.

• Interview With Pharma Analytics Field Application Specialist - Sandi True

  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.

• Leveraging Single-Use Bioreactors In Bench-Scale Process Development

  Scaling bioprocesses requires matching critical variables to ensure consistent cell behavior and product quality. Optimize operations with efficient tools that enable more experiments per year.

• Dry Powder Media Manufacturing Grand Island Expansion

  Take a video tour of our newly expanded dry powder media manufacturing facility in Grand Island, New York. The expansion has added more than 45,000 square feet of Animal Origin Free (AOF) manufacturing space to help meet increasing global demand.

• Accelerating Process Scale-Up From Benchtop To Commercialization- From Controller To Software

  Discover strategies for optimizing process control, refining media selection, and ensuring safety through rigorous contaminant detection to mitigate development risks.

• Supply Chain Efficiency And Sourcing In Gene Therapy

  An overview of the inbound supply chain in gene therapy and the process development challenges that are frequently faced. Learn about concepts such as scaling, cell culture media sourcing, mixing technologies, and configurable packaging.

• Inside Bioprocessing: Microbial Media

  Learn the reasons why the animal origin-free trend in bioprocessing has taken so long to reach microbial bioproduction and the technical hurdles overcome during the development of Gibco CD Bacto Supreme.

• Basic Cell Culture Education Series: CHO Media

  This Knowledge Culture Basic Education Series on CHO media will explore CHO cells: their lineage, historical culture media, and process improvements. We will dive into how to optimize cell culture performance for superior outcomes.

• Cell Culture Media Manufacturing, Paisley, Scotland

  Learn more about our cell culture media manufacturing global network, including details of the Paisley, Scotland site's capacity expansion supporting the bioprocessing industry's rapidly growing needs.

• Cell Culture Media Manufacturing, Grand Island, NY

  Learn more about our cell culture media manufacturing global network, including details of the Grand Island, New York sites capacity expansion supporting the bioprocessing industrys rapidly growing needs.

• Supply Resiliency For Bioprocessing Amid Global Volatility

  Build bioprocessing resiliency with strategic supply chain management. Learn to meet quality, compliance, and time-to-market demands amid global volatility with effective sourcing.

• Streamlining Vaccine Purification: Techniques For Modern Modalities

  Explore cutting-edge chromatography techniques accelerating vaccine purification across diverse modalities, with case studies on HPV, Malaria, and COVID-19.

• Scaling Plasmid DNA Production: A Proven Strategy For Higher Yields

  Learn how an agile manufacturing partner scaled their plasmid DNA production and achieved higher yields by optimizing their media selection and fermentation processes.

• Next-Gen Disease Models And Cell Therapeutics: Innovations In AI, Omics And Collaboration

  Learn how to leverage AI, omics integration, and collaborative research to build more physiologically relevant disease models and accelerate the development of next-gen cell therapies.

• Discover The Benchtop DynaDrive Single-Use Bioreactor

  Ready to transform your process development? Introducing the 5 L Thermo Scientific DynaDrive Single‑Use Bioreactor (S.U.B.), now available! Experience the same bioreactor design from bench to commercial and re‑imagine scalability in process development.

• Efficient Scale-Up Of Monoclonal Antibody Production: From Bench Top To 500L

  Scaling monoclonal antibody production from the lab to a commercial scale can be challenging. Learn about an approach that helps you maintain consistent productivity and product quality across all scales.

• Enhancing Protein Quality Through Optimized Galactosylation

  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.

• Global Strategies For Resilience And Redundancy In Cell Culture Media Supply

  Ensure your cell culture media supply remains uninterrupted. Explore proactive strategies for global manufacturing equivalency and consistent media delivery.

• Tackling Residual DNA Testing In Biotherapy Manufacturing

  Controlling residual host cell DNA is critical for the safety and efficacy of biotherapeutics. Learn about robust, highly sensitive analytical methods for effective DNA clearance and process control.

• Expanding Manufacturing Of Purification Resins To Align With Customer Demands

  Discover how scaling up processes and building out facilities has allowed for end-to-end solutions that meet customer requirements for both supply and quality in their production lines.

• Ensuring Quality, Driving Customer Confidence

  How does quality assurance help drive scientific progress? A 30-year veteran shares her story of supporting customer needs and the development of groundbreaking new therapeutics.

• Enhancing Aseptic Fill-Finish Processes

  Achieve exceptional product recovery and sterility. Learn about high-integrity surge bags, advanced leak detection, and flexible design options for your fill-finish applications.

• Leveraging Rapid Sterility Testing To Advance Cell Therapy Production

  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.

• A Straightforward Path Toward Regulatory Compliance, Data Integrity, And Computer Systems Validation

  Learn practical strategies for validating microbial identification systems in cGMP. Understand regulatory guidance and master a complete Computer Systems Validation plan for full compliance.

• Streamlining Vaccine Development, Production With Modality-Specific Purification Tools

  Novel vaccine purification tools are speeding up development for mRNA, viral vectors, and VLPs. Learn how specific chromatography resins can enhance rapid screening and downstream processing.

• Knowledge Culture: Downstream Innovation

  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.

• Peptones And Vaccines: A Synergistic Approach To Enhanced Production And Efficiency

  Enhance your vaccine manufacturing with peptones. Explore their benefits, analyze data-driven productivity gains, and learn integration strategies in this informative, on-demand session.

• BioTitan Retention Device Overview

  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.

• Advancing Gene Therapy Development With A Multi-Serotype AAV Resin

  In this webinar, leading CDMO ABL and Thermo Fisher will share data on implementation of the POROS™ CaptureSelect™ AAVX affinity resin into such an AAV purification platform, including its performance in purifying several serotypes.

• Maximize Your Drug Product Recovery With A Complete Fill Finish Solution

  Discover how to maximize drug product recovery with an end-to-end fill-finish solution. Get excellent integrity assurance and exceptional lead times for your critical processes.

• Building A Purification Toolkit For An Expanding Variety Of mAb Therapeutics

  Explore techniques for optimizing purification toolkits for various monoclonal antibody formats. This session covers resin and buffer selection for efficient downstream process development.

• Rapid Micro Methods In QC Micro Testing: A NIBRT Perspective

  Learn about some of the advanced Rapid Micro Method systems that are being adopted by biopharma companies worldwide, and how they are changing the face of QC Microbiological testing.

• Simple In-House Mycoplasma Testing Method For Regulatory Expectations And Rapid, Confident, And Actionable Results

  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.

• Analytical Approaches For Quantifying Residual Host Cell DNA

  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.