11.11.26 -- How Is Your Glass Supplier Adapting To Europe's Energy Crisis?

In vivo CAR-T approaches aim to reprogram T cells directly in the body using targeted lipid nanoparticles. Improved delivery to immune organs highlights new potential for scalable cell therapies.

See how scientific process development and QbD principles improve freeze-drying performance, strengthen product stability, and support biologics scale-up.

Excipient selection shapes GLP-1 agonist formulations, from granulated buffers to carrier-based systems aimed at improving solubility and achieving targeted release in the intestine.

Engineering decisions in fill/finish directly shape product quality and sterility assurance. Examine how inert gas purging, plunger placement, dosing verification, and barrier systems interact.

Complex sterile injectables need more than fill-finish capacity. Integrating formulation, analytics, and aseptic filling reduces risk, preserves data, and speeds commercialization.

As complex therapies continue to evolve, advanced lyophilization approaches can help improve stability, consistency, scalability, and product quality.

Eliminate particulate contamination and product degradation in downstream bioprocessing. Learn how frictionless, levitating impeller technology ensures low-shear mixing and high yields.

Maintaining high-quality water for injection is essential for pharmaceutical safety. Discover how strategic design, proactive maintenance, and risk-based monitoring ensure reliable results.

Explore the critical role of pre-use post-sterilization integrity testing in quality risk management, as well as about integrity testing, wetting procedures, and more for effective implementation.

Middlesex County, NJ, offers life sciences organizations a deep talent pool, an extensive R&D presence, and dedicated backing by local government investment.

Unlock superior non-viral CAR T manufacturing outcomes by combining gentle microbubble T cell isolation with advanced electroporation. Find out how this approach boosts cell viability and efficiency.

Read through a demonstration of a rapid CIP being utilized to optimize the loading and non-loading residence times during cycling to achieve increased productivity on a specific capture device.

Sodium hydroxide CIP is essential for column hygiene, but cleaning decisions carry real tradeoffs for resin longevity and long-term chromatography performance.

Observe a new resin designed to simplify antibody purification, improve yield, and enhance contaminant removal during the capture step—ideal for complex therapeutics and GMP workflows.