RECENT WEBINARS
Revolutionizing Cell Metabolism Monitoring
Unlock real-time insights into cell health and productivity with continuous glucose and lactate monitoring. Discover how an innovative technology is transforming bioprocessing and research.
Fulfilling The Promise Of Advanced Therapies And A Noble Cause
Examine how a mission-driven partnership is breaking barriers in cell and gene therapy to deliver faster, affordable access to life-changing treatments for underserved global communities.
The Strategic Advantage of Australia & Asia for U.S. Biotechs
This expert panel explores how Australia, Taiwan, and South Korea provide a strategic advantage in conducting early, mid, and late-phase oncology trials.
Enhancing Protein Quality Through Optimized Galactosylation
Advance your understanding of critical protein engineering. Explore expert strategies for optimizing complex molecular structures, paving the way for more effective and consistent biological products.
Sustainable Vaccine Manufacturing: Securing The Future Of Global Health
Explore how next-gen technologies, from mRNA platforms to digital tools, are transforming vaccine manufacturing to make it more sustainable, flexible, and accessible.
Global Strategies For Resilience And Redundancy In Cell Culture Media Supply
Ensure your cell culture media supply remains uninterrupted. Explore proactive strategies for global manufacturing equivalency and consistent media delivery.
Tackling Residual DNA Testing In Biotherapy Manufacturing
Controlling residual host cell DNA is critical for the safety and efficacy of biotherapeutics. Learn about robust, highly sensitive analytical methods for effective DNA clearance and process control.
Fixing The Monitoring Model: Flexible Resources For Trial Success
Discover how flexible, site-focused monitoring strategies are transforming clinical trials by improving communication, enhancing compliance, and resolving challenges before they impact study success.
Best Practices For PUPSIT Assembly Design And Operation
Navigate the complexities of PUPSIT with expert guidance. Discover best practices for assembly design, regulatory compliance, and troubleshooting common challenges in sterile filtration environments.
CRISPR Meets LNPs: A New Era In Cell And Gene Therapies
Explore how lipid nanoparticles are revolutionizing non-viral gene editing with scalable, efficient delivery for both ex vivo and in vivo applications, which features new CRISPR-LNP data in T cells.
CAR-T Innovation: Balancing Allogeneic And Autologous Cell Therapy
Join experts as they discuss strategies for optimizing allogeneic and autologous therapies, aiming for balanced development and wider patient accessibility by 2030.
Scaling Up Your E. Coli pDNA Process From Parameter Screening To Pilot Scale
Discover a systematic approach to scalable plasmid DNA production using E. coli OneShot Top10, which features DOE-driven optimization and key insights for efficient biomanufacturing success.
What Your Environmental Monitoring Isn't Telling You
Explore overlooked contamination sources, like residues, poor housekeeping, and training gaps, which offer practical strategies to strengthen your contamination control program.
Navigating The New USP Chapter <382> For Elastomeric Closures
Dive into the scope of <382> for pharmaceutical closures and the regulatory landscape. Learn about new required tests and instrumentation for compliance and recommendations on method implementation.
Solving Challenges With Expert Best Practices, Training, And Service
Discover how decades of clinical expertise and cutting-edge automation can streamline your manufacturing workflows, boost consistency, and drive scalable, compliant bioprocessing.
UpTempo℠: Seamless Transitions From Bench To CGT Applications
Accelerate cell and gene therapy development with high-yield, regulatory-compliant plasmid DNA manufacturing that shortens timelines, minimizes risks, and streamlines your supply chain.
Cleanroom Conceptual Design Paradigm: Converting Spaces For GMP Operations Part 2
Learn essential conceptual design principles for transforming alternative spaces into efficient, regulatory-aligned cleanroom environments for your critical processes.
Advanced Contamination Control: Automation, Assays, Process Efficiency
Learn how automated closed systems and larger bioprocess containers contribute to maintaining product integrity and how rapid analytical assays can offer reliable and accurate contamination detection.
Optimize Your Advanced Therapy Manufacturing Process Before You Automate
Dive into specific unit operations and case studies that demonstrate how implementing phase appropriate tools can have substantive direct business impacts to cost and development timelines.
Shaping Therapeutic Development With Cutting-Edge CRISPR Nucleases
Gain an understanding of how an advanced nuclease portfolio is designed to support CRISPR-based cell and gene therapy development, providing scientists with the best solutions for therapeutic success.
Peptones And Vaccines: A Synergistic Approach To Enhanced Production And Efficiency
Enhance your vaccine manufacturing with peptones. Explore their benefits, analyze data-driven productivity gains, and learn integration strategies in this informative, on-demand session.
Building A Purification Toolkit For An Expanding Variety Of mAb Therapeutics
Explore techniques for optimizing purification toolkits for various monoclonal antibody formats. This session covers resin and buffer selection for efficient downstream process development.
Accelerate And Enhance Biomanufacturing Operator Training
Unlock the power of blended operator training and learn how combining digital tools with hands-on instruction reduces errors, boosts retention, and empowers your workforce for real-world production success.
How To Successfully Control The Upscaling Of Your LNP Formulation
Discover key strategies for controlling LNP formulation and upscaling. Explore the science behind lipid nanoparticles, critical parameters, and achieving effective turbulent mixing for optimal outcomes.
Maximizing Media Strategies: Expert Insights On Boosting Performance
Optimize biopharma media strategies for consistent protein quality. Experts discuss formats, variability, and actionable analytics in this on-demand virtual roundtable.
Navigating Regulatory Shifts: EU GMP Annex 1 And USP 382
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.
Mastering The Complexities Of Gene Therapy Document Writing
Gain the insight and strategic flexibility needed to confidently navigate the unique scientific, regulatory, and documentation challenges of gene therapy development.
Optimizing Biotherapeutic Protein Expression With CHO Vector Technology
Review the development of a high-strength synthetic gene promoter that enhances titers while maintaining exceptional product quality and expression stability, to support more efficient biomanufacturing.
Digital Transformation In Contract Manufacturing: A Leadership Perspective
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.
PUPSIT Without The Pain: Practical Solutions For Implementation
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.