Cell and Gene Outsourcing
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Early Preclinical Development: A Successful Transition To cGMP Manufacturing
12/2/2024
Explore the development steps that lead to an mRNA construct optimized for your requirements and that meets future-proof cGMP manufacturing requirements, thereby de-risking the development.
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Optimization-By-Design — A Critical Factor In Viral Vector Scale Up
12/14/2023
Learn how leveraging the expertise and capabilities of an experienced partner is a key factor in optimizing AAV processes using Design of Experiment (DoE), thereby reducing variability and risk.
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Cell & Gene Therapy Development: Characterization Of Cellular Starting Material
6/21/2024
Watch to gain valuable insights into the characterization of cellular source material for the development and manufacture of cell and gene therapy-based products.
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Managing Risks In Injectable Drug Delivery
3/13/2025
Gain insights pertinent to efficient and effective drug development. Understand and execute a risked-based critical thinking approach related to injectable drug packaging and delivery.
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Optimizing Viability And Standardization For Clinical Excellence
10/2/2024
Explore how IntegriCell™ delivers high-quality, manufacture-ready cryopreserved leukopaks, vital for consistent and reliable cell therapy production.
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From Platform To Patient: Streamlining Gene Therapy Development
Explore how platform processes advance gene therapies, the impact of strong partnerships on patient access, and the future shaped by these collaborations.
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A Robust And Scalable Suspension Platform For AAV Manufacturing
Review the demands for AAV manufacturing using a suspension process and the DOE-based strategy used to achieve a scalable process both in terms production and quality of AAV purified.
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The CDMO Value Proposition For Your Autologous Cell Therapy
This panel session features a decade-long story of partnership in bringing two life-changing gene therapies to market successfully in 2022.
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Viral Vector Manufacturing: Improve Efficiency With A Platform Approach
9/25/2023
Learn more about the platform-based scalable suspension process for LVV production and how it is impacting CGTs advancing toward commercialization.
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CRISPR Genome Editing Solutions From Discovery To Clinic
Examine how a partnership leveraging expertise in production for high-quality CRISPR gRNAs as well as cGMP manufacturing is supporting the clinical translation of CRISPR genome editing technologies.