In cell and gene therapy, every step of the workflow, from preservation and cultivation to real-time monitoring, can impact product quality, timelines, and regulatory success.
This webinar will explore how integrated, end-to-end equipment solutions can help CGT teams strengthen reproducibility, reduce operational risk, and simplify day-to-day management across the lab and manufacturing environment.
In this webinar you’ll learn how to:
- Apply preservation, cultivation, and monitoring technologies in a coordinated way to maintain continuity across CGT workflows.
- Strengthen reproducibility using high-quality, CGT-focused equipment and aligned validation and GxP documentation.
- Reduce risk by minimizing disruptions from disjointed systems, equipment variation, and unplanned downtime.
- Simplify support and streamline operations by working with a single partner for training, maintenance, monitoring, and procurement.
Who should attend:
- Lab Operation Manager/Lab Director, R&D Scientist/Principal Investigator
- Clinical Technologist/Operator
- Clinical Lab Manager
- Clinical Lead/Cellular Therapy Director
- QA/Regulatory Affairs Manager, Procurement/Purchasing Manager
- Biorepository Operations Manager
- EHS/Sustainability Manager