On-Demand Webinars
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Removing The Headache: Outsourced Stability Storage And Testing Solutions
12/4/2024
Darryl Souness, Head of Analytical at Cambrex Edinburgh, and Stephen Delaney, Managing Director at Q1 Scientific (a Cambrex Company), share insights on the benefits of outsourcing stability storage and testing.
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Charting A Successful CMC Journey For Your ADC Drug Product
12/3/2024
Learn about best practices and strategies to optimize bioconjugate drug product tech transfers and supplies in clinical or commercial phase, and explore real-world case studies.
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Early Preclinical Development: A Successful Transition To cGMP Manufacturing
12/2/2024
Explore the development steps that lead to an mRNA construct optimized for your requirements and that meets future-proof cGMP manufacturing requirements, thereby de-risking the development.
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How To Boost AAV Titer With Feed Supplementation In Both HEK293 And Sf-9 Platforms
11/25/2024
Explore how optimizing post-transfection or post-infection feeding in HEK293 and Sf-9 cells significantly boosts AAV titers, enhancing production efficiency for gene therapy applications.
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Plasmid DNA For Cell & Gene Therapy: It All Starts Here
11/25/2024
Explore how tailored manufacturing solutions can enhance program outcomes, leverage cutting-edge technologies for research and discovery, and optimize preclinical applications.
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Manufacturing Strategies And Facility Design For Patient-Centric Delivery
11/21/2024
Review how to select the optimal manufacturing strategy and leverage technologies for efficient and scalable production of therapeutic proteins. De-risk the supply chain, accelerate time to market, and reduce costs.
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All Biopharma Roads Begin With Eco-Design: How Can You Get Started?
11/20/2024
Listen to a discussion between Ryan Walker, Cytiva, and Aude Arkam, Sanofi, to learn how the influence of eco-design can guide sustainability in the biopharma industry.
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Scope 3 Emissions: Cut The Complexity With Creative Collaboration
11/20/2024
Delve into the crucial role of Scope 3 emissions in the biopharma industry's sustainability journey, and learn more about the challenges and opportunities of managing these types of emissions.
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Using An Adherent Platform To Scale-Up An Upstream Viral Vector Process
11/20/2024
Gain insight into a helper-dependent adenovirus (HDAd) process that covers everything from bench-scale and optimization to tech transfer.
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Empowering API Manufacturing: Perspectives From A CDMO
11/20/2024
This presentation delves into the critical implications for CDMOs, exploring actionable strategies to bolster API manufacturing capabilities, improve global competitiveness, and support the resilience of European healthcare systems.