MilliporeSigma Webinars
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Effective Supply Chain And QC Testing Through Collaborative Partnerships
9/30/2025
Explore how cross-functional teams streamline cell therapy manufacturing and release for Phase 1 trials to meet patient timelines and ensure safe delivery of personalized treatments.
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Getting Equipped For The Future With A New Microbial Air Sampler
8/25/2025
Discover how a new microbial air sampler meets evolving production demands to enhance compliance, reduce errors, and streamline air monitoring in today’s digital, GMP-regulated environment.
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Navigating The Regulatory Landscape Of mRNA-Based Therapeutics
7/21/2025
Explore the evolving regulatory landscape of mRNA therapeutics in the EU and US, as well as learn key distinctions and strategic opportunities to optimize your mRNA drug development pipeline.
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Practical Applications For Controlled And Safe Nucleic Acid Delivery
7/21/2025
Explore the science behind LNP formulation development, from ionizable lipids to scalable manufacturing through case studies, screening strategies, and flexible approaches for advancing next-generation therapeutics.
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Closed Sampling: Crucial For Aseptic Processing
6/26/2025
Explore the critical role of closed sampling in bioprocessing by gaining insight into regulatory frameworks, system integrity, and aseptic practices essential to ensure compliance and product quality.
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Navigating The Complex Landscape Of Lentiviral Vector Quality Control
6/26/2025
Explore the latest in lentiviral vector release testing, which covers biosafety, regulatory insights, and QC strategies to ensure patient safety and accelerate your path to clinic.
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Accelerate Your AAV Journey To IND And Beyond
6/26/2025
Explore essential QC strategies in AAV gene therapy and learn how to address rcAAV detection, viral clearance per ICH Q5A, and impurity profiling using NGS to meet evolving regulatory demands.
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Purity As A Priority: Optimizing Safety Measures For rAAV Therapies
2/11/2025
Watch to learn how rAAV vectors in gene therapy are addressing manufacturing impurities, risks to patient safety, and analytical methods for detection while aiding sponsors in regulatory compliance.
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Managing Nitrite Impurities: Supplier-Manufacturer View
12/19/2024
Examine nitrites in excipients, nitrosamine risks, regulatory considerations, analytical controls, and a case study on mitigating risks in pharmaceutical manufacturing and storage.
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Demonstrating Technical Excellence In Contract Manufacturing
12/10/2024
Tech Talks explore ADC development innovations, including integrated supply chains, seamless pilot-to-GMP scale-ups, and advanced process analytical technology (PAT).