On-Demand Webinars
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The Increasing Demand For Sterile Filtration Of High Concentration Drugs
3/21/2024
Explore the current trends and challenges with manufacturing high-concentration drug products and an approach to performing extensive filterability trials without a high quantity of expensive product.
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Why KinetiSol® Is Disrupting Spray Drying
3/19/2024
Review a commercially-ready process not only capable of reproducing spray dried dispersions with less manufacturing complexity and environmental impact, but also with the capability to out-design and outperform spray drying.
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KinetiSol® Technology: Scale Up Approach
3/19/2024
Process parameter and quality attribute relationships, including those for typical pre and post KinetiSol unit operations, will be explored in the context of real-world examples.
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Identify And Mitigate Absorption Risks With PBPK Modeling
3/12/2024
See how PBPK models combined with custom and off-the-shelf in vitro tools and solubility enhancement expertise can reduce the need for drug product reformulation or repeated preclinical or clinical studies.
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Selecting Container Closure Systems With Confidence: Lyophilization
3/7/2024
Experts take you through the entire selection process for primary packaging components for lyophilization and provide aspects to consider for all relevant attributes.
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Breaking Bad Manufacturing Habits: Attaining Sustainable API Production
3/6/2024
Sustainability is a growing issue in the pharmaceutical industry. Review strategies for reducing your carbon footprint and learn how the right CDMO can help drive the sustainable manufacture of APIs.
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Building Better Degraders: Targeted Protein Degradation Partners
3/1/2024
Learn from industry experts about the latest advances in chemical building blocks for protein degradation, including warheads, linkers, and ligands, and their role in constructing superior degrades.
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Considerations For Large-Scale API Production
3/1/2024
Explore expert insights on selecting the right CDMO partner for large-scale API production as well as key considerations to ensure your small molecule API program is successful.
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End-To-End Cold Chain Management: A Next-Generation Approach
2/26/2024
Three experts in cold chain management walk through the advantages of end-to-end platforms for bulk drug substance management.
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Understanding ISO/TR 14644-21 Airborne Particle Sampling Techniques
2/22/2024
Industry expert Mark Hallworth guides viewers through the latest ISO document (ISO 14644), exploring the reasons behind the decisions made by the team during its development.