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New Research: Co-Expression Could Make Plant-Based Systems Viable
4/2/2026
By co-expressing Protein A with the protein of interest, the work proposes to reduce the abundant cost of chromatography resins with a one-pot purification approach.
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Quantifying Single-Use Waste Produced During mAb Manufacture
4/2/2026
Discover the current scale of plastic single-use technology waste and its projected growth, specifically for the biomanufacturing domain. There is an increasing need for sustainable solutions.
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The Effect Of Conventional Cooling Versus Controlled Ice Nucleation On Primary Drying Time
4/1/2026
See how controlled ice nucleation shortens lyophilization cycles, supports higher drying temperatures, and reduces complexity for amorphous and mixed formulations without sacrificing quality.
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Scaling MSC Therapies: Overcoming MSC Manufacturing Risks And Barriers
4/1/2026
Explore strategies for scaling MSC manufacturing while mitigating biological and operational risks. Learn how closed-system platforms and optimized workflows accelerate the path to commercial cell therapy.
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From QM To QMM For AI-Assisted Pharmaceutical Manufacturing Operations
4/1/2026
The FDA’s focus has shifted from tracking quality metrics to promoting quality management maturity. AI/ML is poised to help with efforts, though it introduces additional complexity around data integrity.
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The Systems And Choreography Needed For Grade B ATMP Material Transfer
3/31/2026
Traditional material air locks often fail to account for the sheer throughput needed for cell therapy workflows. These design tips help prevent traffic jams.
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Rethinking ATMP Assurance When Sterility Timelines, Reality Misalign
3/27/2026
The compendial 14-day sterility testing window exposes product and patient to numerous risks, but settling on a rapid alternative also presents its own set of challenges.
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Immobilized Enzymes Promise Alternative To Cyanogen Bromide's Toxicity
3/27/2026
Proteases may be more expensive up front, but the benefits of cutting out a highly toxic substance quickly add up when disposal and environmental safety costs go down.
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A Gentler Workflow: Fc-fusion Protein Purification With Mixed-Mode And Anion Exchange Chromatography
3/26/2026
Gain insights into comparative performance, workflow flexibility, and practical considerations for implementing a new weak anion exchange hydrophobic resin and a strong anion exchange resin.
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Selected Drug Product Publications
3/26/2026
Recent studies offer insights on formulation, device compatibility, stability testing, and fill‑finish optimization — helping teams boost product performance and cut development risk.