07.10.25 -- How CGT Leaders Are Reducing Failures, Scaling Processes, And Overcoming Regulatory Friction

A biopharma leader modernized its complex equipment changeover process using an innovative platform to achieve faster execution, fewer errors, and greater visibility through digitized, validatable SOPs.

Change in life sciences is challenging due to strict regulations, high stakes, and the importance of patient safety. Learn how to advocate for digital validation workflows through four key conversations.

Gain valuable insights from digitalization leaders on how some life sciences manufacturers are successfully scaling their Pharma 4.0 initiatives beyond the pilot stage and paving the way forward.

Are your current training methods costly and time-consuming? Explore the benefits of blended learning, which can be up to four times faster than traditional training methods.

Uncover how this expert approach to process transfer supports reliable, scalable commercial manufacturing in the rapidly growing biopharmaceutical market.

Context gives meaning to data, transforming raw numbers into actionable insights, with AI-driven tools that connect data across the manufacturing workflow.

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.

Learn about flexible control software that has revolutionized the way method creation, evaluation, and process optimizations for scale-up are completed.

Delve into the details of this straightforward approach to maximize yields early in development, leveraging vaccine expertise, robust platforms, and Vero and Quail cell lines.

Precision is critical in biomanufacturing. Learn how automated analytical devices are providing real-time, high-resolution data for smarter decision-making and enhanced process control.

What does the BATH-O-CARD acronym represent, and how can it help you during your aqueous cleaning process?

Discover how an innovative single-use microbial impactor revolutionizes contamination control in robotic pharmaceutical filling lines to enhance sterility, efficiency, and compliance in fully automated manufacturing environments.

Utilized wisely, FTZs and subzones can be tools for cost savings and can enable pharma companies to leverage the benefits of American manufacturing.

Explore four common applications of cryopreservation and the science behind selecting the appropriate materials to build single-use solutions that enable cryogenic storage for cell and gene applications.

Sterility in injectable drug manufacturing is vital for patient safety and efficiency. Discover how biofluorescent particle counters revolutionize contamination control, regulatory compliance, and operational excellence in modern pharma.

Surplus and idle equipment can lead to decreases in workspace and work efficiencies for a manufacturing site. Learn how you can get paid for them and clean up your workspaces.