WEBINARS AND VIDEOS

32:54

Practical Solutions For Protein Analytics And Residual DNA Testing

3:08

HyPerforma DS 300 Single-Use Mixer Overview

20:05

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

39:31

Driving Sustainability In Bioprocessing With Biobased Single-Use Solutions

4:24

Interview With Pharma Analytics Field Application Specialist - Sandi True

16:02

Leveraging Single-Use Bioreactors In Bench-Scale Process Development

1:40

Dry Powder Media Manufacturing Grand Island Expansion

41:35

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

20:34

Supply Chain Efficiency And Sourcing In Gene Therapy

15:48

Inside Bioprocessing: Microbial Media

24:48

Basic Cell Culture Education Series: CHO Media

1:28

Cell Culture Media Manufacturing, Paisley, Scotland

• 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.

• Key Considerations For Rapid Microbial Methods For Mycoplasma Detection

  Learn the importance of demonstrating product specific suitability, defining representative sample, consistent sampling protocols, accommodating volume and turnaround time constraints, and the need to establish equivalence.

• Cell Therapy Bioprocessing Workflow Cinematic

  Witness a seamless cell therapy bioprocessing workflow that reduces manufacturing time and preserves the crucial cell phenotype for scalable, effective autologous and allogeneic therapies.

• Implementing Rapid Microbial Identification In Biotherapy Manufacutring

  Learn about rapid microbial identification strategies that enhance environmental monitoring and compliance with regulatory requirements for your manufacturing processes.

• Ultralow Particulate Bottles And Carboys: Where Being Particular About Particulates Is Critical

  Optimize your operations with ready-to-use, meticulously prepared containers. Learn how our commitment to cleanliness reduces risks and supports your most critical requirements.

• Setup Made Simple With The BioTitan Retention Device

  Find out how quick and simple it is to set up an assembly secured with the Thermo Scientific BioTitan Retention Device.

• Successful Microbial Testing And Identification

  In this presentation, one of our industry-leading customers discusses how they've successfully implemented the Applied Biosystems MicroSEQ Microbial Identification System in their laboratory testing.

• ResDNASEQ Workflow Solution

  Explore the Applied Biosystems resDNASEQ workflow solutions. Starting with the sample preparation kit, to purification, quantitating residual host-cell DNA, and analyzing resDNASEQ assays.

• Innovations In Mycoplasma And Sterility Testing For Biopharma

  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.

• CTS DynaCellect Magnetic Separation System Uninstalling Bead Removal Kit

  Safely remove the bead removal kit from the CTS DynaCellect Magnetic Separation System. This video shows you how to remove the cassette and fluid lines.

• CTS DynaCellect Magnetic Separation System Cell Isolation

  Ready to achieve high-purity results in your cell therapy manufacturing? This step-by-step guide demonstrates the complete setup and installation for your automated magnetic cell isolation system and kit.

• CTS OpTmizer One SFM: Thoughtfully Designed Nutrition For T Cells

  Learn about a novel, next-generation medium with an animal-component-free formulation developed to support the need for a T-cell medium that allows consistent, reproducible, and automated T-cell manufacturing.

• An All-In-One Solution For Residual DNA Quantitation

  Explore an all-in-one solution for residual DNA quantitation with a 3D lab tour with virtual demos, videos, and interactive instrument guides to experience the full workflow.

• Maximizing Media Strategies: Expert Insights On Boosting Performance

  Optimize biopharma media strategies for consistent protein quality. Experts discuss formats, variability, and actionable analytics in this on-demand virtual roundtable.