MilliporeSigma Webinars
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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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Addressing Raw Material Handling Challenges By Dry Granulation
8/12/2025
Handling multi-ton quantities of buffers, salts, and stabilizing chemicals in manufacturing can be difficult. Discover how dry granulation improves efficiency, safety, and process reliability.
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Sustainability By Design In API Manufacturing
7/29/2025
Explore the urgent need for sustainability in small molecule API manufacturing, as well as reveal regulatory drivers, green chemistry innovations, and practical strategies to reduce emissions.
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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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Amorphous Stability: Mesoporous Silica For Poor Glass Formers
6/5/2025
Discover how mesoporous silica outperforms polymeric solid dispersions in stabilizing poor glass formers, as well as how it offers a novel approach to enhance amorphous drug stability and bioavailability.
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Unleash The Potential For Polyvinyl Alcohol In Spray Drying
6/4/2025
Discover how polyvinyl alcohol (PVA) addresses key formulation challenges in oral solid dosage forms to enhance solubility and stability across diverse APIs, which include emerging drug classes like PROTACs.
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Little Patients, Big Challenges: Developing Pediatric Formulations
5/12/2025
Explore the development of high-quality, child-friendly oral formulations, as well as learn about new testing requirements for impurities and innovative approaches to creating age-appropriate medications.
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Shaping The Future Of Solid Dose Manufacturing With Hot Melt Extrusion
2/27/2025
Enhance your drug development strategies today and master hot melt extrusion by learning about excipient selection, equipment setup, novel screening tools, and process optimization.
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Nitrosamines - New Requirements To Evaluate Contamination Risks
12/23/2024
Explore nitrosamine contamination, regulatory actions, and new evaluation requirements, featuring expert insights from Dr. Ulrich Reichert on prevention and risk assessment strategies.
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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.