This webinar explores why inspection in HMLV environments is inherently challenging and identifies the most common pain points faced by operations, engineering, and quality teams.
As cell therapy programs transition into clinical development, manufacturing teams face increasing pressure to automate workflows while preserving biological performance and hard-earned process knowledge. Many teams hesitate to introduce automation due to concerns around forced process redesign, loss of flexibility, or risks to clinical timelines. In this webinar, Cytiva specialists will demonstrate how the Sefia™...
During the 2026 BIO International Convention, join Biocom for its highly anticipated Member-Only Bash in partnership with IQHQ—an unforgettable evening bringing together the global life science community. This highly anticipated event brings together professionals from around the world for a dynamic evening of networking, collaboration, and celebration. Set against a stunning waterfront backdrop, Biocom’s BIO...
Bioprocess Online's Bio-Expo Live is back with its series of live virtual events designed to empower biopharma professionals. Through these sessions, attendees will have the chance to explore the newest equipment and solutions offered by our presenters, aimed at addressing the current challenges within the drug development process. This interactive online platform ensures convenience and...
As sterile pharmaceutical manufacturing evolves, isolators and Restricted Access Barrier Systems (RABS) have become central to contamination control strategies across global markets. Yet regulatory expectations from the FDA, EU GMP Annex 1, PIC/S, and WHO differ in meaningful ways, from legal enforceability to technical prescriptiveness, creating compliance complexity for manufacturers supplying multiple markets. This webinar...
Join this webinar to learn how leading cell therapy developers are tackling one of the field’s biggest challenges: scaling non-viral gene-edited cell therapies from research to manufacturing. Through real-world data in T, NK, and CD34+ cells, experts will demonstrate how electroporation can enable efficient CRISPR knock-out, knock-in, and transposon-based editing while preserving critical cell quality...
Womble Bond Dickinson invites you to drop by The Lion’s Share , a beloved San Diego favorite with a speakeasy‑style vibe, for a relaxed reception featuring appetizers, drinks, and great conversation. It’s an easy - and enjoyable - way to unwind and connect after a busy day at the conference. We look forward to raising a glass with you! #BIO2026
Bioprocess Online's Bio-Expo Live is back with its series of live virtual events designed to empower biopharma professionals. Through these sessions, attendees will have the chance to explore the newest equipment and solutions offered by our presenters, aimed at addressing the current challenges within the drug development process. This interactive online platform ensures convenience and...
False rejects are more than a nuisance—they create unnecessary waste, disrupt production efficiency, and erode confidence in inspection systems. In this webinar, we will explore the top 10 causes of false rejects across system setup, environmental conditions, and product and operational variability. We will also demonstrate why false rejects are not inevitable, but instead indicators...
In this webinar, Revvity Signals will explore how Signals Clinical applies governed, fit-for-purpose AI within clinical data review workflows. The discussion will focus on practical ways to accelerate review while keeping clinical experts in control.
