Online webinar

Across biopharma operations, reactive “run‑to‑failure” maintenance is one of the biggest hidden drivers of downtime, deviations, and escalating lifecycle cost. As the industry moves toward digital maturity, organizations are shifting from calendar‑based activities to proactive, engineering‑driven practices that eliminate root causes, strengthen compliance, and create the foundation for future predictive and prescriptive strategies. Proactive maintenance...

Successfully scaling a purification process from development to GMP manufacturing requires maintaining process performance while minimizing variability. However, scale-up often introduces challenges that can impact productivity, recovery, and overall process efficiency. To mitigate risk, manufacturers frequently apply conservative safety factors during scale-up—resulting in lower resin utilization, increased buffer consumption, longer process times, and reduced overall...

A contamination control strategy (CCS) is usually treated as a document with sixteen elements assembled, signed, and shelved. This webinar offers a new perspective of a CCS as a machine that is not so complex that it cannot be analyzed component by component.

In this practical session, Jake Walton, VP of Quality & Compliance at MasterControl, will share a candid look at how MasterControl approached AI the right way from the start—building human-in-the-loop architecture as a non-negotiable design principle, aligning every capability to 21 CFR Part 11, EU MDR, GDPR, HIPAA, and other applicable standards, and going all...

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...

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...

Join experts from Dr. Vince Clinical Research, along with moderator Polly Dawkins of the Davis Phinney Foundation, for a practical discussion on designing and executing successful Parkinson’s disease clinical trials. The session will explore symptomatic and disease-modifying study designs, endpoint selection, emerging research trends and operational challenges. Attendees will gain real-world insights to help advance...

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.

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...