Catalent Cell and Gene Content
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Manufacturing Strategies To Industrialize Autologous Therapies
9/30/2025
Discover how a systematic approach to autologous cell therapy manufacturing can reduce costs, improve reliability, and accelerate access to life-changing treatments.
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Advanced iPSC Workflows: Accelerating Cell Therapy Development
9/30/2025
Beyond offering our GMP-compliant iPS cells, we develop superior workflows for gene editing and differentiation to provide competitive platforms to our partners and accelerate their therapeutic programs.
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Streamline AAV-Based Gene Therapies With Off-The-Shelf Plasmids
8/14/2025
Standardized, well-characterized plasmids and streamlined platform processes can significantly accelerate viral vector development, improve consistency, and support scalable, high-quality gene therapy manufacturing.
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UpTempo℠: Seamless Transitions From Bench To CGT Applications
6/19/2025
Accelerate cell and gene therapy development with high-yield, regulatory-compliant plasmid DNA manufacturing that shortens timelines, minimizes risks, and streamlines your supply chain.
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07.14.23 -- Accelerate Development Timelines With Improved Characterization Methods
7/14/2023
07/14/23 Outsourced Pharma Newsletter
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UpTempo℠ AAV Platform Process
Catalent’s UpTempo℠ AAV platform process is a scalable, cGMP-ready process for viral vector manufacturing that can reduce the current 18-20-month development timeline for drug product in half.
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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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Exploring An Integrated Solution For AAV Vector Clinical Production
Every choice is critical in AAV vector production. Experts share how to make the right choices, from the process and cell line, to off-the-shelf plasmids and qualified analytical methods.
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Accelerating Your Gene Therapy: Not All Platforms Are Created Equal
Standardized methods, materials, and analytics are critical for overcoming hurdles in the gene therapy space. Explore how a platform approach to fast-track AAVs can enhance quality and efficiency.