Cell & Gene Tech Expo offers a live virtual experience designed to empower industry professionals in sourcing best-fit solutions for their cell and gene therapy manufacturing needs. Through this series of digital sessions, attendees will have the chance to explore the newest equipment and solutions offered by our presenters, aimed at addressing the current challenges...
Join Univo IRB for a unique educational webinar that takes attendees inside the IRB decision-making process through a live mock board review. Using a fictional agenda item based on real clinical and ethical challenges, experienced IRB members will evaluate key protocol considerations including risk-benefit assessment, informed consent, participant protections, recruitment strategies, and regulatory compliance. This...
Join Us for the BVS and BioMed Realty Biotech Community Event! Mark your calendars for a great opportunity to connect with industry leaders, explore innovative products, and mingle with fellow professionals in the biotech community. The vendor fair is held at The Forum, in the same building as Amgen and next to Genentech, right in...
The journey from a successful lab result to a reliable, GMP-compliant product is rarely a straight line. It's a transition filled with technical hurdles, regulatory pressure, and the constant challenge of scaling without compromise. We created the Commercial Readiness Solutions session to help you navigate this transition. This virtual event is designed to be highly...
Unexpected particle findings can raise critical questions about product quality, patient safety, and regulatory compliance. Join KBI Biopharma's experts to learn how clinical in-use studies and advanced particle forensics can help identify particle sources, assess risk, and build regulator-ready evidence for confident decision-making. Register now to discover practical strategies for accelerating investigations, supporting development timelines,...
As biologics developers work to improve productivity, maintain product quality, and accelerate development timelines, traditional optimization approaches can sometimes reach a point of diminishing returns. While cell culture processes generate vast amounts of biological and process data, extracting actionable insights from that information remains a significant challenge. In this webinar, Thermo Fisher Scientific specialists discuss...
As biologics developers work to improve productivity, reduce development timelines, and manage manufacturing costs, traditional media optimization approaches can become increasingly resource intensive. Predictive modeling is emerging as a complementary approach that can help integrate biological knowledge, process data, and artificial intelligence (AI) to support more efficient media development. In this webinar, Thermo Fisher Scientific...
Nanoparticle programs can stall when early formulation choices fail to hold up through scale-up, tech transfer, and manufacturing. Join leading CDMO experts on August 18 at 11:00 AM ET to learn how decisions around lipid or polymer selection, particle engineering, process design, and manufacturability can impact downstream success. Register now to gain practical insights that...
Oral solid dose programs can run into costly scale-up challenges when early formulation and process decisions aren’t built for long-term manufacturability. Join leading CDMO experts on August 18 at 1:00 PM ET to explore how excipient selection, granulation strategy, particle engineering, and process design can impact tech transfer, validation, and commercial manufacturing. Register now to...
In this webinar we expand on some of the processes most vulnerable to introducing titer variability, as well as strategies to overcome sources of variability when they are unavoidable to maintain high-titer production.
