The key to unlocking maximum OEE? Integrating dosing accuracy, platen sealing, magnetic shuttle transport, and automated 100% in-line quality control into a unified workflow. Join our virtual event, "How to...
Mesenchymal stromal cell (MSC) therapies are entering a pivotal stage of development. As more programs move toward late-stage clinical trials and commercialization, developers must produce enough high-quality cells to meet...
Lipid nanoparticles (LNPs) are critical to the delivery of genetic medicines, but developing scalable, reproducible manufacturing processes remains complex and resource-intensive. Because LNP quality can be highly sensitive to formulation...
Strategies for supply assurance, QC readiness, digital optimization, and commercial bioprocessing success. The translation of cell culture processes from laboratory-scale development to commercial manufacturing remains one of the most critical...
Join us for an exclusive webinar exploring practical strategies to improve therapeutic antibody manufacturing through integrated upstream and downstream process solutions. As therapeutic antibody titers continue to rise, manufacturers face...
As the December 1, 2026 release of the revised USP <87>, Biological Reactivity Tests, In Vitro, approaches, pharmaceutical and medical device manufacturers should begin evaluating how these changes may impact...
A risk-averse investment climate has made it more difficult for startups to find the funding needed to bring novel treatments into the clinic. However, alternative funding sources, investment models, and...
Virtual Pharma Expo - a themed event featuring presentations and demonstrations by leading experts from pharmaceutical equipment providers for oral solid dose manufacturing and packaging.
Innovations in self-administered and wearable drug delivery technologies promise convenience but bring questions about how to effectively monitor and manage patient safety, adherence, dosing accuracy, and, ultimately, medical outcomes. In...
Transitioning development processes into GMP manufacturing can come with a fair share of growing pains. Development teams need to contend with things like sourcing and validating new materials, ensuring regulatory...
