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CELL AND GENE THERAPY ANALYTICS

46:00 Scientists in lab-GettyImages-1441665026
Innovative Contamination Control: Enabling Integrity And Efficiency

An integrated approach can enhance contamination control, boost process efficiency, and ensure the production of high-quality cell therapy products.

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.

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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.

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Scaling Viral Vectors

Industry experts cover the high operational costs associated with viral vectors, along with the challenge presented by their shot shelf life and scalability.

2:39 resdnaseq workflow
ResDNASEQ Workflow Solution

Overview of the resDNASEQ workflow solution.

48:11 Digital Solutions For Accelerated Innovation
Digital Solutions For Accelerated Innovation

In this webinar, hear how Applied Biosystems AccuSEQ software serves as an advanced digital tool that can help streamline bioanalytical processes and accelerate the delivery of life-changing therapies.

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Overcoming Capacity Constraints

How can CGT biotechs overcome issues such as building an in house facility and ultimately get their therapies to patients.

43:12 Successful Microbial Testing And Identification
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.

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.

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.

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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.

30:09 Innovative Strategies For Residual DNA And Viral Titre Quantitation
Innovative Strategies For Residual DNA And Viral Titre Quantitation

Discover how digital PCR improves the accuracy of residual host cell DNA and viral titre quantification in biotherapeutic manufacturing to enhance product quality, safety, and regulatory compliance.

24:19 Maximize Quality Assurance Through Rapid Sterility Testing
Maximize Quality Assurance Through Rapid Sterility Testing

This webinar explores mitigating the risk of product loss, and production delays, as well as the critical role rapid sterility testing plays in ensuring the quality and safety of cell therapy products.

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.

24:54 GettyImages-505636269 titer
Analytical Solutions To Help Accelerate Bioprocessing Success

Unlock the power of data-driven bioprocessing. Discover how advanced analytics can optimize your cell culture process, improve performance, and accelerate success.

40:02 Thermo - webinar
Rapid Process Development And Technical Support For AAV Scaleup

Accelerate your AAV production journey. Learn how rapid process development and expert support can streamline your path from vial to purified bulk, ensuring scalable and efficient manufacturing.

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Manufacturing Hurdles With Viral Vectors

With a wide range of viral vector-based drugs already approved, viral vectors are expected to remain the primary delivery mechanism for the foreseeable future. However, as the demand for viral vectors increases, addressing the challenges related to their manufacture and s...

0:26 resDNASEQ Cinematic
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.

5:17 BPI Interviews Purification And Pharma Analytics Leader
BPI Interviews Purification And Pharma Analytics Leader

Jean Luo, VP of Purification and Pharma Analytics, discusses innovations in bioprocessing, including the development of dPCR assays, lentiviral titer systems, chromatography resins, and supply chain.

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Quality Control Assays

Two company leaders detail not only the vectors their respective companies use and why but also the quality control assays performed on viral vectors.

0:20 Explore The Analytics Knowledge Hub
Explore The Analytics Knowledge Hub

Discover smarter solutions with the new Analytics Knowledge Hub that provides articles, webinars, e-books, and infographics designed to enhance and streamline your bioprocess workflow.