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WEBINARS

34:48 Thermo - 7-23-25 webinar
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.

44:08 A Successful Journey To Cell Therapy Manufacturing
A Successful Journey To Cell Therapy Manufacturing

Learn about the three main areas to consider when you're preparing to commercialize a cell therapy, including starting/raw material, the controlled manufacturing process, as well as testing safety and quality.

53:13 Thermo - next gen disease models webinar
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.

41:39
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.

18:56 Enhancing AAV Purification In Gene Therapy Manufacturing
Enhancing AAV Purification In Gene Therapy Manufacturing

Review chromatography solutions for purifying multiple AAV serotypes, with specialists’ insights on bioprocessing and downstream optimization.

9:51 Cell therapy workflow
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.

25:28 Multi-Omics And Bioinformatics In Cell Culture Media Design
Multi-Omics And Bioinformatics In Cell Culture Media Design

Learn about the impact of a multi-omics analysis, utilizing proteomics and metabolomics, in the development and optimization of media with the goal of improving titer, and making development and manufacturing more efficient.

27:52 Thermo - Regulatory webinar
Navigating Global Regulatory Landscapes In An Evolving Biopharma Industry

Minimize regulatory risks and ensure compliance in the evolving biopharma sector. Watch this on-demand discussion for insights on change management, supplier collaboration, and future market trends.

1:44:46 CHO Solutions Day Part 1
CHO Solutions Day Part 1

This CHO Solutions Day presentation offers valuable insights into new media and feed systems, a successful scale-up story, and how multi-omics analysis can enhance your cell culture.

57:25 Microbial Identification Via DNA-Seq
Microbial Identification Via DNA-Seq

Learn how DNA sequencing-based microbial identification supports regulatory compliance and enhances contamination control in critical environments.

32:54 Thermo Fisher - QC webinar
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.

33:20 Using Residual DNA Quantification Data To De-risk mAb Development Bucket
Using Residual DNA Quantification Data To De-Risk mAb Development

Residual DNA quantitation offers more than impurity measurement. When used across process steps, it helps compare purification performance, identify risks early, and ensure assays remain reliable.

1:03:39 Rapid Micro Methods In QC Micro Testing
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.

59:11 Manufacturing Considerations For Viral & Non-Viral Platform Selection
Manufacturing Considerations For Viral & Non-Viral Platform Selection

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.

20:50 Scalable Purificaiton Of In Vitro Transcribed mRNA
Scalable Purification Of In Vitro Transcribed mRNA

Learn more about how affinity-based mRNA chromatography resin facilitates the purification and isolation of mRNA from in vitro transcription (IVT) manufacturing processes.

42:06 Rapid Prototyping Through cGMP
Accelerating Cell Culture Media Manufacturing: From Rapid Prototyping Through cGMP

Industry leaders addressing effective ways to help streamline media manufacturing, including rapid small scale non-cGMP media prototyping and proprietary media formulation outsourcing options.

33:13 Purification Tools To Address Low Yield Challenges With Protein A
Purification Tools To Address Low Yield Challenges With Protein A

Discover new affinity chromatography resins for engineered modalities. Learn how they boost yield and reduce aggregation with high-specificity binding and mild elution. Ideal for purifying novel mAbs, BsAbs, and mAb fragments.

4:24 Interview With Pharma Analytics Field Application Specialist - Sandi True
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.

28:57 How Modular Workflows Are Redefining CAR T Manufacturing
How Modular Workflows Are Redefining CAR T Manufacturing

Learn how flexible modular workflows can help manufacturers improve process adaptability, throughput, and control while preserving key CAR T quality attributes, including transduction efficiency.

44:04 Thermo - Future of Single Use webinar
Digital Design Meets Proven Performance: The Future Of Single-Use Assemblies

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.

29:20 Streamlining Vaccine Purification TFS thumb
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.

46:24 Validation Of A qPCR Assay For Host Cell DNA Quantitation
Validation Of A qPCR Assay For Host Cell DNA Quantitation

Here, we share the development and validation of a new, highly sensitive and accurate integrated solution for detection and quantitation of host cell DNA to help meet regulatory requirements.

33:07 Manufacturing Friendly Aggregate Clearance In Downstream Processing
Manufacturing Friendly Aggregate Clearance In Downstream Processing

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.

18:11 DoE Methodology For Downstream Purification Of pDNA Of IEX Resins
DoE Methodology For Downstream Purification Of pDNA Of IEX Resins

Learn a systematic approach using Design of Experiment to optimize plasmid DNA purification. See how anion exchange resins are evaluated to enhance dynamic binding capacity and process efficiency.

11:59 aavx magnetic beads purification
Efficient AAV Purification With AAVx And AAV9 Magnetic Beads

Explore an alternative to chromatographic affinity capture that eliminates the need for universal nuclease treatment by utilizing magnetic beads with ligands specific to AAV.

28:28 Supporting Development Of mRNA Therapeutics By Enabling Commercial-Scale
Supporting Development Of mRNA Therapeutics By Enabling Commercial-Scale mRNA Purification

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.

56:12 Thermo Fisher - Downstream Processing webinar
Tools For Efficient Downstream Processing Of Antibody-Based Therapeutics

Watch and discover how to effectively utilize chromatography tools for improved purification of therapeutic monoclonal antibodies and antibody derivatives.

29:39 Implementing Rapid Microbial Identification
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.

14:27 Optimization Of Anion Exchange Purification
Optimization Of Anion Exchange Purification For The Large-Scale Production Of Plasmid DNA

In this webinar, we discuss pDNA purification, including how to identify optimal conditions for various chromatography media and optimize recovery and impurity removal.

37:50 GettyImages-1296140220 virus, lentivirus
Scalable Production Of Lentivirus For Research To Commercial Manufacturing

Join our webinar on scaling the CTS LV-MAX System in bioreactors, covering transfection scalability, Thermo S.U.B. advantages, and DynaSpin’s efficient gene therapy integration.