Bioprocessing White Papers
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Streamline Your AAV Process With A Production Platform
10/6/2025
AAVs are reshaping gene therapy, but scaling production introduces complexity. Learn how upstream process optimization can improve yield, consistency, and speed to meet growing demands.
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Achieve Higher Targeted Concentrations
9/30/2025
Single-pass TFF streamlines downstream processing by reducing footprint, shear exposure, and hold-up volumes. Learn how this approach is advancing efficiency across therapeutic and vaccine production.
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Improving Methodologies For iPSC Manufacturing And Differentiation
9/30/2025
Learn how next-generation workflows are being developed to streamline iPSC manufacturing, enhance differentiation strategies, and overcome the hurdles of scalability and consistency.
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Innovation And Evolution Of Affinity Chromatography Resins For Monoclonal Antibody Purification
9/30/2025
Discover how innovations in ligand design and resin manufacturing have improved monoclonal antibody purification by enhancing selectivity, stability, and process economics.
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Molecular Approaches To Streamline Cell Therapy Product Analytical Testing
9/26/2025
Learn how rapid molecular methods of cell therapy testing like qPCR for mycoplasma, sterility, and lentiviral quantification are key to accelerating product release and timely treatment delivery.
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Beyond Traditional Monoclonal Antibodies
9/24/2025
New antibody formats present new purification challenges due to novel impurity profiles. New methods and media are required to ensure safe, effective, and scalable manufacturing of these biologics.
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Optimizing Charge And N-glycan Profiles For CHO-Derived Fusion Proteins
9/24/2025
Discover how structured design-of-experiment approaches can optimize charge variants and glycosylation to enhance biologics quality and therapeutic performance.
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A Comparative Analysis Between Liquid Nitrogen And Mechanical Freezers
9/23/2025
Explore the differences between liquid nitrogen and mechanical cryogenic freezers, and learn how each method supports scientific, medical, and industrial storage needs.
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A Risk-Based Approach To Plasmid DNA And mRNA Process Development
9/23/2025
Balancing robust analytics and clinical readiness is key for early-phase pDNA and mRNA therapeutics amid structural complexity and regulatory challenges.
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Optimize DNA Clearance In High-Salt, GMP-Grade Purification Processes
9/16/2025
Efficient hcDNA removal is vital for therapeutic safety and compliance. Discover how salt-active enzymes support high-salt purification workflows to help manufacturers meet strict regulatory standards.