Biologic Outsourcing STREAM
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Delivering Top Quality Fill Finish Manufacturing
Bringing an innovative parenteral drug product to market requires a fill finish manufacturing partner with the resources and solutions to deliver top quality products and the agility to meet your needs.
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AGC Biologics Capacity Update October 2025: Large Molecule
10/16/2025
Michael Brotz provides an in-depth look at our Seattle site and the unique capabilities of the facility, including its single-use and stainless-steel capacity, new manufacturing lines, and more.
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Biotherapy Characterization: Binding Assays
7/17/2019
MilliporeSigma Senior Scientist Helen Hsu, Ph.D. describes how, with our custom binding assays, and supported with our comprehensive off-the-shelf Fc gamma receptor binding assays, we can help you optimize your mAb production, from clone development through upstream and downstream processes.
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New Protein A Device Set To Redefine Biomanufacturing
3/25/2025
Discover how the Gore Protein A Membrane Device, in collaboration with AGC Biologics, can revolutionize your manufacturing processes, enhancing efficiency, scalability, and innovation from discovery to GMP-level production.
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Step Inside One Of America's Leading Protein Biologics CDMO Sites
9/3/2025
Take a behind-the-scenes look at AGC Biologics’ Seattle campus, one of the most established and productive CDMO facilities in the United States.
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MilliporeSigma Capacity Update October 2025: Large Molecule
10/16/2025
Our global facilities are built to guide you when you’re ready to scale; and power your mRNA journey from discovery to global commercialization.
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Streamline Your mRNA Purification Steps
3/4/2025
Ensure your mRNA's stability and effectiveness post-transcription with advanced filtration and chromatography techniques to enhance purity and recovery, which delivers high-quality mRNA for superior therapeutics and vaccines.
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Meet The Experts: PAT, Raman Spectroscopy, And Chemometrics
4/14/2023
Gain a better understanding of process analytical technology (PAT), Raman spectroscopy, chemometrics, and Raman applications in bioprocessing.
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ICH Q7 Good Manufacturing Practice Guide For Active Pharmaceutical Ingredients
6/7/2022
The ICH Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients is the most commonly referenced quality guideline in pharmaceutical product and contains five segments. Watch the video to learn more.
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MilliporeSigma Bio-Expo Live February 2025: Downstream Bioprocessing
3/17/2025
Advancements in single-use technologies are transforming antibody-drug conjugate manufacturing and offering increased flexibility. Examine key data, design considerations, operational benefits, and applications in ADC production.