RECENT WEBINARS
Five Practical Considerations To Move From Concept To Clinic
Learn more about five key factors for advancing targeted in vivo LNP programs, from formulation and targeting strategies to bioanalytical readiness and scalability.
Overcoming Regulatory Hurdles In AAV Production
Demonstrating residual reagent clearance is a critical regulatory requirement in AAV manufacturing. Explore how specialized assays and strategic partnerships streamline compliance.
From Lab To Commercialization: Simplifying Bioprocess Scale-Up
Explore how unique cuboid geometries and advanced mixing dynamics create consistent performance from the bench to commercial manufacturing, ensuring flexibility and improved productivity.
CRO Selection Science: Insights From $2B+ Vendor Choices
Discover how data-driven strategies and structured RFPs can simplify CRO selection, improve transparency, and ensure the right operational fit. Learn practical steps to make smarter vendor decisions.
Seal The Deal: Mastering Vent Integration In Medical Devices
Learn how precise vent placement and microfiltration design optimize performance in life science devices. See practical troubleshooting strategies and a real-world case study.
Lessons From FDA 483s And Warning Letters: Cleanroom Compliance
Learn critical lessons from FDA 483 observations and Warning Letters to proactively address common GMP cleanroom compliance failures and build an inspection-ready facility.
Robust And Cost-Effective mRNA Capping
Master the essential strategies for cost-effective and robust mRNA capping at industrial scale. Learn how to successfully evaluate new materials and optimize your synthesis process for maximum efficiency and yield.
Eliminate Risk From Your Viral Vector Tech Transfers
Explore strategies to simplify viral vector tech transfers, reduce risk, and maintain quality under tight timelines, as well as a case study that demonstrates how to streamline this critical process.
Navigating Innovation And Challenges In CGT Bioprocessing
This expert panel breaks down the practical realities of today’s supply chain while forecasting how emerging technologies will redefine quality standards.
Navigating Regulatory Expectations For Injectable Packaging
Explore insights on extractables, focusing on how they relate to the revised EU GMP Annex 1, new and evolved expectations under USP <382>, and the use of VHP decontamination in aseptic environments.
Cleanroom Changes In 2026 For Better Contamination Control
Proactively improve your cleanroom strategy for 2026. Gain actionable insights on leveraging Environmental Monitoring data, optimizing personnel, and managing residue to enhance contamination control.
Critical Path For Gene Therapy: AAV Analytical Lifecycle Considerations
Explore considerations for phase-appropriate AAV characterization and release activities from pre-clinical to late-phase products. Review validation challenges and paths for maturation of analytics.
Raising The Bar In Gene Therapy
Learn how a science-driven and digitally structured approach reduced onboarding timelines for gene therapy from 12 months to just 3, setting a new benchmark in technology transfers.
Smart Media Screening And Design: Saving Time And Boosting Titers
Optimizing your cell culture media selection is crucial for clinical advancement. Learn how high throughput screening techniques accelerate media and feed optimization to significantly boost your biologics' titers.
Addressing The Challenges Of LNP Upscaling
Overcome LNP upscaling challenges by leveraging fluid mechanical principles. Learn how Impingement Jets Mixing achieves reproducible turbulence and consistent LNP quality across all production scales.
Streamlining pDNA: Capacity, Complexity, And Cutting-Edge Solutions
Learn how flexible facility design and process innovation are accelerating pDNA manufacturing, as well as key strategies to avoid scale-up pitfalls and meet growing therapeutic demand.
Are You Keeping Pace With Oligo Synthesis Optimization?
The rapidly expanding oligo market demands optimized RNA synthesis. Examine key innovations and workflow insights to maximize resources and control long-term manufacturing costs.
Accelerate Your pDNA And mRNA Process Development
Explore a structured approach to optimizing and scaling plasmid DNA production using E. coli, with insights into key growth parameters, benchtop feasibility, and pilot-scale performance.
Practical Solutions For Protein Analytics And Residual DNA Testing
Discover practical solutions for common quality control bottlenecks in biotherapy manufacturing. Learn how to improve protein analytics and DNA testing robustness and accelerate time to market.
Choosing The Right Sporicide: Critical Factors For Robust Cleanroom Contamination Control
Choosing the best sporicide for your cleanroom involves evaluating factors like surface format, contact time, and safety. Learn the criteria to select an effective and robust agent for contamination control.
Boosting Vaccine Yields Through Smarter Cell Culture Media Optimization
Unlock efficient vaccine production by understanding how tailored peptone supplementation optimizes cell culture media, improving cell growth and overall yield across multiple critical cell lines.
Navigating Commercial Cell Therapy Manufacturing
Explore expert insights on manufacturing strategies, quality management, scalable production, and digital tools that enhance collaboration and ensure consistent, efficient multi-product facility operations.
Driving Sustainability In Bioprocessing With Biobased Single-Use Solutions
Discover how biobased materials in bioprocessing enable measurable carbon emission reductions. Learn practical strategies to meet decarbonization goals and adopt greener, operationally sound practices.
Enhancing Viral Vector Sterile Filtration: Process Efficiency And GMP Alignment
Explore filtration strategies that improve viral vector yield and quality, with insights on AAV and lentivirus workflows, plus practical guidance for implementing PUPSIT in line with requirements.
The Future Of Gene Therapy Production: Enriching Full Capsids, Reducing Costs
Explore how intensified upstream processing enriches full AAV capsids, reduces impurities, and lowers manufacturing costs. Learn how extended culture duration drives better outcomes.
Developing Your Risk-Based Approach To Single-Use System Integrity
Explore how a holistic approach to single-use system integrity can strengthen contamination control, improve operational efficiency, and meet evolving regulatory expectations in manufacturing.
Optimize DNA Clearance In High-Salt, GMP-Grade Purification Processes
Explore how salt-active endonucleases overcome DNA clearance challenges in viral vector purification by digesting down to 3–5 nucleotides and performing reliably in high-salt conditions.
The Case For Optimized And Excipient GMP Cell Culture Solutions
Learn how optimized, customizable formulations and Excipient GMP manufacturing streamline development, ensuring quality and consistency for a de-risked path to the clinic.
Enhancing Non-Viral CAR T Manufacturing With Electroporation And Microbubble T Cell Isolation
Unlock superior non-viral CAR T manufacturing outcomes by combining gentle microbubble T cell isolation with advanced electroporation. See how this approach boosts cell viability and transfection efficiency.