Events

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.

How can life sciences companies developing new medicines engage the FDA successfully during a period of rapid changes in agency personnel and policies? Should companies adjust their agency communication strategies or ask new questions during meetings? Our deeply experienced panelists will discuss key changes at the FDA, how companies can get the most out of...

Explore how leading teams are using trusted data and targeted AI to design, plan, and execute trials with the confidence today's science requires. Learning outcomes: - Understand what's driving trial complexity - Design protocols with confidence using real data + AI - Select sites based on holistic drivers of outcomes; access, experience and past performance...

Join Dr. Marco Davila to explore a novel anti-CD83 CAR-T design for relapsed/refractory AML that overcomes myelosuppression barriers. Register for the live session. Developing effective Chimeric Antigen Receptor (CAR) T-cell therapies for Acute Myeloid Leukemia (AML) remains one of the most formidable frontiers in cellular immunotherapy. Unlike lymphoid malignancies where lineage-specific targets like CD19 or...

Join us for a practical discussion on selecting the right Container Closure Integrity Testing (CCIT) method for your container system. Learn how deterministic and probabilistic approaches compare, understand the impact of package design and product characteristics on method selection, and gain a risk-based framework for justifying your CCIT strategy to regulators.

Achieving consistent upstream performance remains a critical challenge as bioprocesses become more complex and quality expectations continue to rise. From variability in raw materials to maintaining cell growth, productivity, and product quality across platforms, process developers are under increasing pressure to build more robust and reliable manufacturing processes. Join this webinar to explore practical strategies...

Explore data from an end-to-end CAR-T workflow using cryopreserved leukopaks. This session will examine how key process parameters affect cell recovery, viability, consistency, and scalability across washing, cryopreservation, thawing, and final formulation. Attendees will learn practical strategies for defining operating ranges, reducing variability, and building more robust closed-system autologous manufacturing workflows.

A practical framework for reducing variability, minimizing manual sampling, and improving run-to-run consistency with modern UF/DF control strategies. August 26, 2026 | 11:00 AM ET Ultrafiltration Diafiltration (UF/DF) is often treated as a straightforward concentration and buffer-exchange step, but teams know the reality looks different. Small differences in setup, endpoint definition, and in-process decision-making can...

Are you making the most of your time at CPHI Milan? Watch this free virtual event to evaluate CDMOs, CMOs, API suppliers, packaging providers, and other outsourcing partners before you arrive onsite. Gain early insight into supplier capabilities, compare potential partners, and build a focused meeting strategy that maximizes your time at CPHI Milan. Register...