March Cytiva Webinar

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.

Bridging The Gap Between Product Readiness And Equipment Availability

Discover how manual precision at scale bridges packaging gaps, accelerates product launches, and ensures uninterrupted supply to deliver quality when automated equipment isn’t yet operational.

Automating Visual Inspection Qualification

Transferring visual inspection data from paper to digital is essential for Pharma 4.0 compliance. Learn practical strategies to eliminate errors, automate data tracking, and enhance quality assurance.

When A Logbook Project Becomes A Digital Movement

A leading pharma company accelerated execution and compliance in GMP operations. See how modular apps replaced manual processes, setting a new foundation for continuous innovation.

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.

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 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.

Extrusion-Based ASD Scale-Up: Performance Through Process Understanding

Explore the formulation and manufacturing considerations for amorphous solid dispersions (ASDs), with a focus on hot melt extrusion (HME) as a scalable and cost-effective technology option.

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.

EU GMP Annex 11: Compliance Strategy And Digital Solutions

Explore how EU GMP Annex 11 revisions could reshape global pharmaceutical compliance, as well as strategies for navigating implementation challenges and building future-ready validation programs.

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.

From Readiness To Results: Unlocking Capacity For Expanding Product Demand

Learn the six pillars that bridge operational readiness and operational excellence. Discover a proven framework to build a resilient, high-performing manufacturing operation and unlock necessary capacity.

Advancing Topical Formulations With Innovative Preclinical Models

A robust formulation development approach integrates scientific principles, systematic formulation development, and preclinical models to facilitate early identification of candidates with poor developability.

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.

Driving Robust Tech Transfer In Biologics: CFD Simulation

Computational Fluid Dynamics simulation is essential for robust biologics tech transfer. See how this predictive tool optimizes critical scale-up processes, reducing risk and expediting time to market.

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.

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.

Achieve Pharma 4.0 With Next Generation Software-Defined Manufacturing

Explore how software-defined manufacturing is helping companies overcome legacy system challenges, improve OEE by up to 25%, and accelerate batch release cycles while maintaining compliance.

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.

Innovations, Solutions, And USP <1062> With Scale Up

Optimize tablet compression by simplifying calibration, speeding up changeovers, and utilizing advanced laser inspection to prevent critical punch tip wear and maintain quality.

Faster Tech Transfers Through Seamless Digital Transformation

Manual process documentation slows innovation. Learn how modular libraries and digital connectivity enable faster, error-resistant execution, bridging the gap between process design and automation.

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.

How To Address Your Solid Dosage Processing Needs

Unlock the keys to consistent solid dosage products. Learn to align unique product needs with optimal processing requirements and equipment strategies. Gain a roadmap for improved quality and reproducibility.

Smarter CMC Strategies To Accelerate Next-Gen Biologics To The Clinic

Learn how process design and cross-functional collaboration mitigate risks and accelerate the path from early development to FIH manufacturing through real-world case studies of practical approaches.

AI In Action: Driving Operational Excellence In Life Sciences

Discover how combining domain expertise with advanced AI and data engineering automates compliance, accelerates readiness, and provides real-time insights for confident decision-making.

Integrated Manufacturing To Mitigate CMC Risks, Simplify Commercial Supply

Leveraging cross-functional coordination between sites, harmonized tech transfers, one quality system, and synchronized team activities can streamline regulatory submissions and deliver high-quality commercial outcomes.

Driving Operator Safety And Process Efficiency

Discover how ergonomic design and workflow simplification can turn routine production tasks into strategic advantages, as well as practical ways to boost safety, efficiency, and innovation.