Production
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How To Choose A Capping Method In MRNA Production
2/24/2023
Is your mRNA production process ready for scale up? Learn how to choose a capping method to optimize your mRNA yield and process costs.
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Improve The Performance Of Your Small And Large Molecule Medicines
7/23/2024
Explore the latest in nanotechnology advancements including recent clinical data, formulation applications, and API optimization to NanoImprove formulations.
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Developing Modular Facility Proof-Of-Concept For Multi-Modal Bioprocessing
2/2/2023
Learn about the innovative solution of designing and constructing manufacturing facilities using predesigned and prefabricated elements.
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The Future Of mRNA Manufacturing
Watch to explore a box solution that provides flexible and scalable options for your mRNA workflows and is designed to support the evolving landscape of mRNA production.
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How To Plan For Trouble-Free Filter Validation
10/28/2024
Watch to learn when filter validation should be performed, what is required from an end user and laboratory testing perspective, and how to achieve first-time success for various drug products.
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Strategies And Emerging Technologies For mAb Capture
3/8/2022
Explore opportunities with the introduction of high-capacity protein A resins, how and when multicolumn chromatography is beneficial, and how emerging technologies can address bottlenecks.
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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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Workflow For Rapid Sterility Testing
4/14/2023
Learn about the workflow for an automated solution for the rapid detection, imaging, and quantification of viable microbial contaminants in filterable samples at various stages of the manufacturing process.
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Technology To Overcome Absorption Hurdles And Solubility Limitations
3/6/2024
For poorly soluble drugs, overcoming absorption hurdles can hinder development. Explore a solution that empowers researchers to overcome solubility limitations and accelerate drug development.
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How To Develop An Efficient Downstream Purification Process For bsAbs
5/1/2023
Bispecific antibodies (bsAbs) have gained increasing interest in recent years. Learn how to develop an efficient downstream purification process for a cancer immunotherapy bsAb.