Outsourcing STREAM
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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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Collaboration & Expertise, The Keys To Efficiency And Scalability Across All Modalities
7/8/2022
View this video and discover our global vaccine capabilities from process development to full-scale GMP-manufacturing and in all modalities.
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Thermo Fisher Scientific North America Single-Use Technologies Capacity Expansion
3/2/2021
Thermo Fisher Scientific is expanding our single-use manufacturing network globally. Some of the largest investments are taking place at our existing Logan, Utah, and Millersburg, Pennsylvania, sites. We are adding space for clean rooms for the manufacturing and assembly of Thermo Scientific BioProcess Containers and fluid transfer assemblies, investing in 2D and 3D chamber manufacturing equipment, and harmonizing our quality systems and processes.
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Partner With A CDMO For Your Biologic Commercial-Scale Manufacturing
3/18/2022
Discover how our full-service biologics CDMO can help you navigate the journey from clinical to commercial drug substance manufacturing and provide tailored guidance and solutions.
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Increasing The Reach Of Cell And Gene Therapies
4/29/2021
The cell and gene therapy industry is rapidly evolving from the perspective of “can we commercialize this class of therapeutics?” to “how do we reach patients who need these therapies?”. However, the promise of these biologics can only be realized if the industry approaches manufacturing parity with monoclonal antibodies. A mixture of innovation and brute-force streamlining is needed to create viable cell and gene therapy templates. In this video, we discuss how upstream process optimization is ripe for innovative approaches.
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The Journey To Safety Through Viral Clearance
12/1/2022
Discover a simple yet powerful solution for getting viral clearance studies done safely, thoroughly, efficiently, and on your timelines. Learn how to free your teams and trust your project.
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Raman PAT Platform – Model Building Support Animation
11/16/2021
Interested in implementing Raman as a PAT tool to monitor your bioprocesses in-line and in real time? But not a chemometric expert? Our experts are here to support you! Watch this video to learn more.
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Optimize The Formulation Of A Monoclonal Antibody
12/11/2019
You have a molecule of interest and need an effective formulation to maximize stability and minimize aggregation. As with all formulations, it is essential that the buffers and excipients ensure stability of the drug substance, be compatible with each other and meet regulatory requirements. An emerging biotech company sought our help in developing a formulation for a monoclonal antibody. Learn how we have delivered an optimized formulation for this customer in three months.
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How MilliporeSigma Promotes Quality And Risk Reduction
10/20/2021
Learn how MilliporeSigma’s new facility was built with quality and risk reduction at the top of mind and its experts have the experience to support large-scale programs through commercialization.
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Accelerate Identification Of High-Producing Cell Lines
12/11/2019
When companies are putting in place an upstream process, a critical step is generation of a cell line expressing the protein of interest. Unfortunately, the search for the best-producing clone is often compared with looking for a needle in a haystack. Watch our video to learn about our mini-pool approach and the value of automated systems to efficiently create, screen and isolate high producing clones with reduced costs.