What does it take to turn breakthrough biology into successful in vivo therapies? As innovations in synthetic biology, RNA editing, and gene therapy continue to accelerate, vector design and manufacturing...
In some ways, it has been a quiet(er) year on the regulatory front for mRNA; there have been no mRNA-specific guidances released since the MHRA personalized cancer immunotherapy guidance and...
As biologics, complex injectables, and stricter regulatory requirements reshape sterile manufacturing, facility design has become a critical factor in operational success. In this webinar, learn how purpose-built modular aseptic filling...
The trend toward 3D printing in process development is driven by early-stage benefit: engineers can create custom equipment for scale-up and scale-down initiatives and mitigation of process integration challenges. When...
This webinar gives clinical research sites a practical look at how AI is being used today across source documentation, regulatory compliance, finance, eSource, and other site operations. CRIO’s Mike Wenger...
Early ADC development often requires critical decisions to be made with limited data and scarce material. In this webinar, discover a streamlined analytical approach that enables accurate measurement of antibody-drug...
This 2-hour virtual showcase gives clinical teams a faster, easier way to evaluate patient recruitment and retention partners. Attendees will hear short capability presentations, compare providers side by side, and...
Discover how a simple redesign of the AAV helper plasmid could make gene therapy manufacturing more efficient and cost-effective. In this webinar, Samsung Biologics shares how its promoter-optimized mini-helper plasmid...
CRO change orders can quickly become difficult to manage once a study is underway, especially when budget revisions, approvals, comments, and financial projections are spread across emails, spreadsheets, and disconnected...
This expert panel will discuss how digital documentation is reshaping inspection readiness. Panelists will explore the role of electronic batch records, integrated quality systems, and automated workflows in supporting compliance...
