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Adherent Cell Manufacturing & Process Development
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Analytical Method Development and Validation – Building the Characterization Testing Foundation & Toolkit
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Augmenting Automated Analytics for Cell & Gene Therapy Manufacture
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Closed, automated and controlled upstream processing for iPSC-derived cell therapies
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Data Governance and Data Integrity as a framework during Process Development
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Fresh vs. Cryopreserved: Tightening up Supply Chains
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Manufacturing and quality control of cell therapies
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PANEL: COVID-19: Trailblazers in the CGT Industry
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Phase Appropriate Thinking – Microbiology and Contamination Control
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Process Development Considerations for Exosomes
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Product Dependent Cryopreservation Protocols
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Sourcing Appropriate Starting and Ancillary Materials for Manufacturing Cell and Gene Therapy Products
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Tracking from Donor to Patient
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Delivering on the Promise of Producing Cost-Effective, High-Quality Allogeneic Immune Cell Therapies
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Development of modern biologics and cell therapy products through global CMOs
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Implementation of “off the shelf” Closed Systems fit for every purpose
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Non-Gene Edited Approaches to Allogeneic CAR-T Cell Therapy
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Optimizing Viral Vector Production
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PANEL DISCUSSION: Partnering Solutions for Staffing and Recruitment Issues in the CGT Space
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PANEL DISCUSSION: Spinning out from Academia and Ensuring early stage success
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PANEL: Autologous Manufacturing – What will Autologous Manufacturing of the Future Look Like?
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PANEL: Investment in the CGT space: trends, technologies and early stage success
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PANEL: Reimbursement Models for Novel Therapies
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PANEL: Strategies and Challenges in Manufacturing and Commercialization
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Pathogen Safety Margins for Gene Therapy Manufacturing
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Scalable Manufacture Platform of Human iPS-NK Cells for Off-the-Shelf Cell Therapies
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Starting Material Standardization for Auto and Allo Cell Therapies
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The Case for rAAV Titration by HPLC
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The Potential CAR-NK
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TAC T-cells leverage the Natural TCR’s properties, Have an Improved Safety Profile Compared to CAR-T cells and are Efficacious in Solid Tumors
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Efficacy/Toxicity Linkage with CAR and T Cell Therapies
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Cytokine modulation of CAR-T cells to improve their safety and efficacy
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Overcoming Cell Therapy Limitations with Next Generation Approaches based on Natural Killer Cells
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Standardization & QC for Gene Editing
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Developing allogeneic CAR T-cells that lack host reactivity and can resist rejection to improve their safety and persistence
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