MilliporeSigma Webinars
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Collaborative Bioprocessing: Next-Gen mAb Downstream Manufacturing
9/23/2024
Explore the bioprocessing template, operational paradigm, and the complexities of qualifying an advanced, highly automated bioprocessing train designed for the production of mAbs and other biologics.
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What Do You Need To Do To Qualify A Single-Use Assembly?
8/28/2024
Learn about the implementation of single-use technologies, single-use user requirement specifications, and best practices for single-use qualification, including quality and regulatory documentation.
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Navigating Cleanroom Compliance For Safe Material Transfer
7/23/2024
Watch to explore various aspects of environmental monitoring essential for the transfer of materials into controlled areas as well as recent advancements that can facilitate this task.
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How To Accelerate And Enhance ADC Therapies
6/24/2024
Learn how payloads and advanced payload intermediates can expedite drug development and elevate ADC therapies, and explore ADC payloads, payload intermediates, and solubility-enhancing technology.
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Make More Lentivirus And Make It Right The First Time
6/14/2024
Discover how you can achieve higher titers and robust yield with an optimized, end-to-end lentivirus platform, designed to maximize production and quality for the success of your cell or gene therapy.
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Filling The Sterility Testing Gap: Traceability And 21 CFR Part 11 Compliance
6/6/2024
Watch to learn about a solution that offers digital information for every stage of a sterility test while remaining compliant with 21 CFR Part 11.
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Strategic CMC Planning Through A Phase-Appropriate Quality Approach
5/28/2024
A phase-appropriate quality approach ensures quality activities align with the unique risks and challenges of each development phase. Watch how to apply such an approach to CMC planning.
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Unleashing The Power Of Perfusion In Intensified Processes
5/28/2024
Explore the advantages of implementing a perfusion-specific CLD process to produce more productive clones as well as an integrated solution for intensified processing.
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Key Quality Attributes For mRNA Drug Substance Performance
5/23/2024
Explore the evolution of the mRNA-based therapeutics pipeline, and gain insights into the key quality attributes and associated analytics that influence mRNA performance, including best practices.
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How To Bring Your LNP Formulation To Clinical/Commercial Manufacturing
5/23/2024
Gain valuable insights into key considerations when selecting lipid excipients for LNP formulations and the process development steps necessary to advance them to GMP manufacturing and clinical trials.