Biopharma Research & Scientific Content
Explore our library of informative resources including white papers, scientific articles, research posters and on-demand webinars.
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Browse the content below for insights into the future of the biopharma industry, Q&A's with scientists, research results on new innovations in biotech, information on the benefits of CDMO's, and new drug development and manufacturing techniques.
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eBook: Guide to CDMO Outsourcing for Biologics
Outsourcing for Beginners - Biologics, mRNA, and Beyond
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Technical Note: Membrane Technology in Protein A Affinity Capture
Overcoming Barriers to Adopting Membrane Technology by Demonstrating Protein A Affinity Capture Step Product Quality and Process Characteristic Similarity
![Hydrodynamic shear and turbulent flow gore white paper - download graphic](https://www.agcbio.com/hs-fs/hubfs/Whitepapers/Hydrodynamic%20shear%20and%20turbulent%20flow%20gore%20white%20paper%20-%20download%20graphic.png?width=573&height=653&name=Hydrodynamic%20shear%20and%20turbulent%20flow%20gore%20white%20paper%20-%20download%20graphic.png)
Technical Note: Understanding the Effects of Hydrodynamic Shear & Turbulent Flow
Hydrodynamic Shear and Turbulent Flow Considerations for High Productivity Membrane Affinity Chromatography
![Cystine and tyrosine feed in CHO cells article - download graphic](https://www.agcbio.com/hs-fs/hubfs/chub_backup/Cystine%20and%20tyrosine%20feed%20in%20CHO%20cells%20article%20-%20download%20graphic.png?width=896&height=1021&name=Cystine%20and%20tyrosine%20feed%20in%20CHO%20cells%20article%20-%20download%20graphic.png)
Research Article: Production Process Improvements of Antibody Drugs
Cystine and tyrosine feed reduces oxidative and ER stress in CHO cells
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eBook: 12 Must-Read Biopharma Case Studies
Engineering challenges and practical solutions by expert Naveenganesh Muralidharan
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Research Article: Productivity Factors in Antibodies
Antibody Productivity of CHO Cells is Altered by ER Stress Tolerance of the Host Cell
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Webinar: Gene Therapy Development For Regulatory Approvals
Successfully validating your LV gene therapy product process to gain FDA and EMA approval
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Cell & Gene Therapy PPQ and Process Development
The Fast Lane to Market: A 3-Stage Exploration of CGT Process Development
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Q&A: Examining the Future of Manufacturing Cell Therapies
The Next Frontier: Industrializing Cell Therapy Manufacturing
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Adeno-Associated Viral Vector Cell Line Development Q&A
Cell Line Development for AAV with AGC Biologics' Upstream Vector Development Manager, Silvia Ungari
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Article: Accelerating CGT with Plug-and-Play Viral Vectors
Accelerating the Cell and Gene Therapy Journey with Plug-and-Play Viral Vector Production Platforms
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Webinar: New Protein A Purification Technology
Unpacking the Resin Alternatives: Single-Use Protein A Tech that can Reduce Costs and Accelerate Your Clinical Journey
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The Future of Microbial Manufacturing
From Petri Dish to Profit: 5 Changes Driving the Future of Microbial Drug Manufacturing
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Webinar: Large-Scale Viral Vector Manufacturing
Bridging the Distance to Large-Scale GMP Manufacturing of Viral Vectors
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R&D Cell Line Development Q&A
Prioritizing R&D Initiatives to Support Biologics Cell Line Development
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Webinar: Cell Therapy Strategies
Building Flexible End-to-End Cell Therapy Manufacturing Strategies
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Research Poster: Downstream LVV Purification
Downstream Strategies for Concentration and Purification of LV Vectors from Suspension Cell-Based Systems
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Study: Protein A Capture Membranes vs. Resin Columns
Building a Fully Single-Use Process: High Productivity Protein A Membrane Devices that Complement Disposable Upstream Technology
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PATs for Improving Inline Monitoring
Q&A: How PATs Improve Bioreactor Performance and Inline Monitoring
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Webinar: Gene Therapy Challenges
Gene Therapy Development: Navigating Economic Challenges & Regulatory Changes
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New Market Opportunities for mAbs
Monoclonals Revolutionizing Pathogen Treatments
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Natural Killer Cells
The Promise of NK Cells and 3 Strategies for Creating a Cost-Effective Program
![Giuliana Vallanti mini webinar video thumbnail](https://www.agcbio.com/hs-fs/hubfs/Webinars/SME%20Video%20-%20Giuliana%20Vallanti%20Extended%20mini%20webinar%20video%20thumbnail.png?width=430&height=490&name=SME%20Video%20-%20Giuliana%20Vallanti%20Extended%20mini%20webinar%20video%20thumbnail.png)
Mini webinar: Regulatory & Quality in Cell and Gene
Expert, Giuliana Vallanti, discusses regulatory approvals and quality challenges
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Eliminating Downstream Bottlenecks
Eliminating Downstream Bottlenecks and Boosting Productivity in Antibody-Based Therapies
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Scale-Down Models
Get to GMP Clinical Stage Quickly Utilizing Scaled-Down Models in Viral Vector Production
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Allogeneic Cell Therapy
Opportunities to Accelerate Allogeneic Cell therapy Production
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Webinar: Cell Line Development
On-demand webinar: Accelerating Cell Line Development from DNA to Master Cell Bank
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Large-Scale AAV Manufacturing
Manufacturing Large-Scale AAV From Concept to Ready-to-Use Platform
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Custom Viral Vectors
Like a Tailored Suit: Producing Customized Viral Vectors that Respond to Market Demands
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Mammalian Large-Scale Commercial Manufacturing
Q&A: Outsourcing Mammalian Development & Large-Scale Commercial Manufacturing
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pDNA Upstream Optimization
The Future of Plasmid DNA Upstream Optimization
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PPQ Assessment
Assess Reliability, Confidence, Inter & Intra Batch Variation Uncertainties in PPQ Sample Size Selection
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mRNA Custom Program
mRNA: How to Build a Custom Program Using CDMO Services
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cGMP Compliance
cGMP Compliance in a Growing Biologics Market
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Webinar: Large-Scale AAV Manufacturing
On-demand webinar: The Future of Plug-and-Play Large-Scale AAV Manufacturing
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Process & Tech Transfer
Manufacturing Process Transfer: Understanding Challenges & Keys to Success