06.18.26 -- Inside AstraZeneca's Fully Electrified Cell Therapy Facility

Learn about the role of single-use technology in advanced therapy manufacturing, why pharmaceutical manufacturers are switching to disposable technology, and more.

Explore how low-volume purification can be done more efficiently in GMP settings with a live system demo and customer insights on optimizing workflows with single-use chromatography.

Scaling gene therapy demands precision and actionable data. Discover how integrated technologies like ultracentrifugation and mass spectrometry enhance AAV yield, purity, and characterization.

A new functionally-closed cell expansion system featuring a hollow-fiber membrane and customizable protocols is streamlining the production of stem cells for regenerative medicine.

This study demonstrates how a low-shear, closed-system centrifuge achieved over 90% MSC recovery and minimized viability loss, supporting scalable cell therapy manufacturing.

Review the foundational manufacturing principles of LV vectors alongside essential testing frameworks, focusing specifically on replication-competent virus and infectious titer assays.

Uncover how evolving regulatory pathways and CMC innovation are shaping the future of gene therapy and viral vector production, plus what these mean for selecting a CDMO partner.

Flow electroporation streamlines VLP manufacturing for gene editing applications. This technical data highlights scalable production methods that maintain consistent editing potency.

Choosing the right incubator requires more than reading specs. Check out these tips for evaluating performance metrics, contamination control, and real-world functionality to make confident equipment decisions.

Gain insight into the nuances of cleanroom conceptual design for GMP operations and see how an integrated approach can ensure regulatory compliance, functionality, and environmental performance.