pharm-stream-recent-webinars
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Maximizing Media Strategies: Expert Insights On Boosting Performance
5/22/2025
Optimize biopharma media strategies for consistent protein quality. Experts discuss formats, variability, and actionable analytics in this on-demand virtual roundtable.
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Navigating Regulatory Shifts: EU GMP Annex 1 And USP 382
5/20/2025
Strengthen risk mitigation strategies while ensuring regulatory alignment. Gain valuable insights into best practices and proactive approaches for building a robust and future-ready CCS.
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Utilizing A Stepwise Approach For Nitrosamine Risk Mitigation
5/15/2025
Insights and case studies demonstrate how a tailored, stepwise testing approach can effectively detect, quantify, and control nitrosamine impurities while maintaining cost efficiency.
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Digital Transformation In Contract Manufacturing: A Leadership Perspective
5/13/2025
Discover how PCI Pharma Services embraced digital transformation and gain expert insight on overcoming challenges, driving innovation, and maintaining core values in a regulated industry.
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PUPSIT Without The Pain: Practical Solutions For Implementation
5/6/2025
Explore the critical role of pre-use post-sterilization integrity testing in quality risk management, as well as learn about integrity testing, wetting procedures, and innovative filtration systems for effective implementation.
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Accelerating Technology Transfer Through Unified Recipe Management
4/30/2025
See how a unified recipe authoring workflow can reduce technology transfer times in manufacturing, enhance validation efficiency, and streamline operations by integrating process control systems.
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From Cell Line Development To Upstream Optimization: Enhancing Biologics Quality And Productivity
4/30/2025
Explore how advanced cell line development and upstream processing strategies optimize both productivity and therapeutic effectiveness, ensuring the development of high-quality biologics.
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3D Screen Printing: Breakthrough Solutions For Patient-Centric Therapies
4/29/2025
Explore 3D screen printing’s potential to revolutionize pharmaceutical manufacturing with scalable, customizable, multi-drug tablets and precise, patient-centric drug release profiles.
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Inside The Development Of An AAV8 Production Platform
4/24/2025
Explore innovative solutions for AAV8 production challenges, which include scalability and purity, as well as learn how a collaboration with CDMO Matica Biotechnology ensures efficient, high-yield gene therapy vector production.
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Sustainable Manufacturing Through Efficient BioProduction Unit Operations
4/23/2025
Delve into the critical environmental and economic aspects of bioprocessing. Explore the urgent need to manage the industry’s growing plastic waste issue and a three-pronged approach to address this challenge.