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COMMERCIALIZATION AND LOGISTICS

5:05 Perfusion Hardware Needs
Perfusion: Hardware Needs

In this video, we will discuss cell retention mechanisms, pumps, and intensification challenges in the perfusion process.

5:02 Thermo Fisher Scientific Suzhou, China Manufacturing Site Capabilities
Thermo Fisher Scientific Suzhou, China Manufacturing Site Capabilities

Watch this video to learn more about this manufacturing site capabilities, quality management systems, PPI implementation, product expansion, assurance of supply and lead times.

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.

21:45 Leveraging dPCR r Techniques To Quantitate Lentivirus Particles
Leveraging dPCR r Techniques To Quantitate Lentivirus Particles

Discover how digital PCR can streamline lentiviral vector characterization to reduce variability and improve analytical sensitivity. Learn how this approach can help you comply with regulatory guidance.

28:59 Thermo - 7-17
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.

9:07 24_04_CGL_1920x1080p_Seg4
Defining The CMC / Clinical Relationship For Allogeneic Cell Therapies

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.

40:39 GettyImages-1170605838 quality
Quality Roundtable: Raw Material Planning For Tech Transfer And Scaling Biologics

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.

37:20 Key Considerations For Rapid Microbial Methods For Mycoplasma Detection
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.

15:32 Cell And Gene Therapy Innovations
Cell And Gene Therapy Innovations

This interview with a pharmaceutical analytics expert discusses key insights into advances in cell and gene therapy and the strategies used to support customers in improving their therapeutic development.

1:28 TruBio Software Performing A 2-Point Calibration
Master The 2-Point Calibration Process To Maintain Data Integrity

Ensure accurate sensor readings with an innovative software by mastering the 2-point calibration process. Learn more about how and why regular calibration supports data integrity and compliance.

6:10 23_07_CGL_COGS_Webinar_Seg06
Safety And Efficiency Of Source Material Collection

Expert CTO's detail how automation improves safety and efficiency when collecting source material.

1:15:45 AAV Purification
AAV Purification: Solving Downstream Challenges

In this roundtable discussion, a trio of distinguished experts in AAV purification and process development share their expertise and best practices in tackling and solving downstream challenges.

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.

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.

1:05:00 GettyImages-1181190018 supply chain pharma, bio
The Way Forward: Supply Chain Solutions

Learn how to build a resilient supply chain to navigate today's complex environment. Expert speakers share insights on optimization, innovation, and strategic planning to meet evolving market conditions.

7:55 23_09_CGL_ViralVector_Webinar_1920x1080_Seg03
Regulatory Compliance And Viral Vectors

Hear from experts who detail the specific regulatory challenges for advanced therapies, as well as how the regulatory requirements differ in early research and development in academia and in industrial vector production.

2:10 TruBio Software Performing A Single Pump Calibration
TruBio Software: Performing A Single Pump Calibration

Confidently manage your bioprocessing systems with precision and ease by learning how to calibrate a single pump using innovative software, which ensures accurate fluid delivery.

43:39 Innovations In Mycoplasma And Sterility Testing For Biopharma
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.

3:46 Thermo Screen splash
Singapore Single-Use Site Capacity Expansion

Thermo Fisher Scientific is expanding our single-use manufacturing network globally, an expansion site closer to Asia Pacific region

2:48 23_09_CGL_ViralVector_Webinar_1920x1080_Seg04
Market Demand For AAV Vectors

Here, Dave Maheu, VP, Head of Process & Analytical Development at Candel Therapeutics and Curran Simpson, Chief Operating Officer at REGENXBIO detail the key factors driving the adeno associated virus manufacturing market.

43:42 Simple In-House Mycoplasma Testing Method
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.

11:39 23_12_CGL_mRNA_Webinar_Seg06
mRNA For Cancer Immunotherapy 2024 Outlook | Audience Q&A

During our Cell & Gene Live, mRNA For Cancer Immunotherapy 2024 Outlook, our expert panelists answered audience questions regarding patient safety, foreseeable challenges in mRNA cancer immunotherapy for solid tumors, and much more.

4:19 Perfusion Medium Selection And Testing
Perfusion: Medium Selection And Testing

An examination of what to consider in a perfusion medium, including varying reconstituted concentrations, supporting multiple cell clones, allowing for high cell densities at low medium exchange rates, and using it in various types of perfusion.

1:49 Bioprocessing Equipment And Automation Product Portfolio Overview
Bioprocessing Equipment And Automation Product Portfolio Overview

Accelerate biotherapeutic development with innovative bioprocessing equipment and automation solutions that feature single-use mixers, bioreactors, and more to streamline workflows and speed products to market.

8:53 23_07_CGL_COGS_Webinar_Seg05
Auto, Allo, And AI

CTO experts debate autologous and allogeneic, and how automation improves the CAR-T cell process every step from collection to infusion. They also discuss the major ways AI optimizes automation.

3:39 Thermo Fisher
Thermo Fisher Scientific Single-Use Global Manufacturing Network

We have implemented a multi-tier strategy to improve the resiliency of our supply chain and created the largest networked single-use manufacturing organization in the world.

20:34 Supply chain efficiency
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.

0:43 Dynacellect Cinematic Overview
CTS DynaCellect Cinematic Overview

Achieve high cell purity and recovery with an automated, closed magnetic separation system. Learn how this technology helps increase robustness, minimize failures, and streamline cell therapy manufacturing.

6:22 23_07_CGL_COGS_Webinar_Seg02
Technology Needs For Automated Manufacturing

Investigate the importance of technology as it relates to automation and standardization within cell therapy manufacturing. The panelists in this discussion cover solutions and services needed for process automation in CGT.

32:04 Isolating CD4  CD8 T Cells For Improved Drug Efficacy, Productivity
Isolating CD4 / CD8 T Cells For Improved Drug Efficacy, Productivity

Learn how the active detachment of dynabeads from target cells at any time allows users to add flexibility and scalability to their process.