On Demand Webinars
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Evolving Into Biopharma 4.0: A Stepwise Journey Of Digital Transformation
8/29/2024
You don’t need to make huge investments to shorten time-to-market. Watch to discover how incremental steps can transform your processes using digitalization and automation.
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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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Maximize Quality Assurance Through Rapid Sterility Testing
9/10/2024
This webinar explores mitigating the risk of product loss, and production delays, as well as the critical role rapid sterility testing plays in ensuring the quality and safety of cell therapy products.
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How mRNA Manufacturers Disrupt The Industry
3/21/2023
Learn how biopharmaceutical companies can apply proven strategies to overcome hidden complexities in mRNA production, and discover solutions that can help you rapidly design and build a SU facility.
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Regulatory Guidance For Bioprocessing Software
2/9/2022
Gain an understanding of the regulatory requirements for software in a biopharmaceutical GxP environment and how software is invaluable for creating an audit trail, reporting, and automating regulatory-related tasks.
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Accelerating Clinical Development In China & The US
9/22/2022
Discover how the clinical research bridge between China and the US supports accelerated clinical development from early to late phase trials while ensuring the inclusion of MRCT data packages in future regulatory applications.
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RNA Interference - From Single Gene Studies To Whole Genome Screens
11/7/2022
Endoribonuclease-prepared siRNAs (esiRNAs) are able to overcome the limitations of RNAi. Learn about esiRNAs, their advantages over standard siRNAs, and ways this technology is utilized in different research fields.
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Early Phase Excellence: Navigating B Cell Therapies In Autoimmune Conditions
12/2/2025
Watch as expert panelists share insights into the most critical considerations for navigating early-phase clinical development and designing studies that reliably translate mechanisms into meaningful patient outcomes.
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Sustainable Approaches To Oligonucleotide Manufacturing
An industry expert shares about sustainable Oligo manufacturing approaches that can save time, cost, and resources – while improving purity, quality, and scalability of these promising therapeutics.
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The Role Of Peptones In Boosting Quality And Yield
11/4/2024
Peptones can significantly boost CHO cell bioprocessing. We analyze their impact on diverse CHO cell lines using real-world data to assess their effects on titer, protein quality, and cell growth.