On-Demand Webinars
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Future-Proof Your Aseptic Filling
2/24/2023
Using the Cytiva SA25 Aseptic Filling Workcell, a standardized system designed with flexibility built in, ensures that companies can pivot between products quickly and adapt as manufacturing needs change.
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Addressing Key Challenges Of High Concentration Formulation Development
High concentration formulations often present challenges with regard to viscosity as well as potential changes in the behavior upon stability. Discover solutions to mitigate high viscosity.
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Development And Scale Up Of Insoluble, Microbially Expressed Biologics
Delve into the use of inclusion bodies within biopharmaceutical production, which are now gaining attention for their potential in producing a range of difficult to express proteins in E. coli systems.
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Formulation Of Crystalline Nanoparticles Enabling Superior Drug Load
8/13/2024
Explore how bioavailability of poorly soluble APIs can be improved and patient compliance enhanced by reducing the size or number of tablets that a patient must take to achieve the required dose.
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Scale-Up And Production Of Key Lipids Used In mRNA Delivery Systems
2/13/2025
Discover key strategies for overcoming challenges in the industrial-scale production of ionizable and PEG lipids to optimize mRNA vaccine formulation and address critical manufacturing requirements.
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Dry Powder Inhalable Vaccines For Shelf Stability And Global Access
6/3/2024
What if a formulation that removed the need for cold chain distribution was possible? Explore the formulation of vaccines and manufacturing considerations for dry powder inhaled vaccines.
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Solving For Solubility: A Scale Up Strategy For Spray Dried Dispersion
Spray drying offers a solution to formulation challenges for enhancing the bioavailability of poorly soluble APIs but requires technical capability and operational excellence to accomplish the process successfully.
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Pharmaceutical Spray Drying: Sustainable Commercial Best Practices
Learn more about defining the spray drying process with an emphasis on specific enhancements to accommodate scale-up to commercial scale equipment of challenging applications or molecules.
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EU Med Device Regulations: Ensuring Compliance For Integral Combination Products
Review the EU Medical Device Regulation (MDR) changes, specifically with respect to integral combination products, and examine the technical documentation packages supporting functionality and content.
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Formulating Better ASDs And mAbs: Advances In Applied Nanotechnology
5/1/2024
Learn about new data on nanotechnology formulations for multiple dose forms and routes of delivery, including oral, long-acting injectables, inhalation, and ophthalmic.