Events

Pediatric gene therapy is rapidly reshaping what is possible for children born with rare genetic diseases. Join Dr. Rachel Abu Taleb, Medical Director, Medical Affairs at Veristat, for a look...

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...

Looking for fill-finish manufacturing capacity? This webinar brings together leading CDMOs to showcase their latest sterile filling, lyophilization, and advanced packaging capabilities, along with current facility availability and timelines. Gain...

Explore the latest large molecule manufacturing capabilities from leading CDMOs in this informative webinar. Learn about advances in cell line development, fermentation, purification, process optimization, and scale-up, while gaining insight...

As cell therapies advance toward commercial-scale manufacturing, developers can face increasing pressure to balance performance, scalability, and process flexibility. Flexible modular workflows are emerging as a powerful approach for scalable...

Technology transfers can introduce risk and create knowledge gaps at every stage of development, whether it’s moving a process from development to manufacturing, transferring methods between analytical labs, or onboarding...

Moving promising research from the university lab to the CDMO suite requires more than breakthrough science—it requires the right documentation, development strategy, and manufacturing readiness. In this Outsourced Pharma Live...

In this virtual event, leading CDMOs will share how host selection, vector design, and clone screening strategies influence manufacturability from early development through commercialization. Join us to learn what to...