On-Demand Webinars
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Utilizing Flow Cytometry For Humoral Immunogenicity Testing: Cell & Gene Therapy
9/29/2025
Discover strategies to overcome immunogenicity challenges in cell and gene therapies, with a focus on harnessing flow cytometry to enhance ADA and NAb assay development, strengthen validation, and ensure regulatory readiness.
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Filtration Unfiltered: Technology To Meet New Bioprocessing Challenges
9/29/2025
Explore how filtration strategies are adapting to diverse molecule pipelines, regulations, and sustainability targets with insights into process intensification and the technologies shaping the future.
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Future Of Pharma Packaging: Trends, Tech, And Patient Solutions
9/25/2025
Explore how traditional and innovative pharmaceutical packaging formats improve patient adherence, support emerging therapies, and shape the future of drug delivery and treatment outcomes.
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Not All Manufacturing Automation Is Created Equal
9/25/2025
Learn how outcome-based automation helps life sciences manufacturers reduce risk, improve performance, and drive measurable results—by aligning tools with business goals.
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Streamlining Biologics Development: Leveraging Small-Scale Studies For Greater Efficiency
9/25/2025
Uncover how a data-driven approach to small-scale studies not only accelerates development timelines but also enhances decision-making and resolves full-scale manufacturing challenges across diverse biologic modalities.
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Mobilizing Science, Partnership, And Capability To Develop A Gene Therapy In 14 Months
9/17/2025
Hear how one family, driven by urgency, partnered with AAV experts to develop a treatment for their daughter’s ultra-rare neurodegenerative disorder, NEDAMSS, in just 14 months.
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Nanoforming Biologics, GLP-1s: From I.V. To Sub Q And Inhaled Delivery
9/9/2025
Developing new delivery routes is essential for creating more effective treatments. Nanoforming enables new routes to simplify dosing, enhance patient comfort, and reduce healthcare costs.
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Managing Endotoxins - Detect, Prevent, Remove
9/8/2025
Explore the risks of endotoxin contamination in drug manufacturing and discover sustainable, animal-free detection methods to ensure pharmaceutical safety and regulatory compliance.
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Benefits Of Outsourcing To An Integrated CDMO
9/8/2025
Streamlining ADC development through an integrated CDMO can reduce risk and improve quality. Discover why specialized expertise in linker chemistry and bioconjugation is key to overcoming the complexity of ADC manufacturing.
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Extractables, Leachables, And Risk: Ensuring Safety In Pharma Manufacturing
9/8/2025
This session is designed for teams developing new products, optimizing processes, or preparing regulatory submissions, and will provide practical tools for a better approach to E&L management.