Optimizing End-to-End CGT Workflows: Integrated Equipment Strategies to Reduce Risk and Strengthen Reproducibility

Webinar Date: July 16, 2026
Time: 1 pm ET
Duration: 1 Hour

 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

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PHC Corporation of North America
Product Manager for Cell Culture
PHC Corporation of North America
Chief Innovation Officer
Image Mike Auerbach
Editor-in-Chief
Pharmaceutical Outsourcing