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Session Details

Managing the First Mile from Collection to Cryopreservation: Standardizing Starting Material Requirements
Wednesday, May 29, 2024 08:00 AM - 09:00 AM  
Room 202-204
Roundtable
Organized by: ISCT Process Development & Manufacturing Committee

Moderator(s)   
  • Lizette Caballero, BS, MT(ASCP), Johnson & Johnson Innovative Medicine, United States
  • Dominic Clarke, PhD, Cryoport Systems, United States
Panelists
  • Joseph Schwartz, MD, MPH, Moffitt Cancer Center, United States
  • Kathy Loper, MHS, NMDP, United States
  • Tracey L. Hlucky, CQA, CMQ/OE (ASQ), Kite Pharma, United States
CenterBridge differences in processes, practices, and strategies across collection sites and sponsors to enable consistency and scalability.

Key Learning Objectives:

1. To understand the impact of collection practices on downstream preservation.
2. Which components of the cryopreservation process are most critical.
3. Discuss and identify the need for creating best practices for collection and cryopreservation of the leukapheresis starting material.

 

Lizette Caballero
Associate Director-CTL
Janssen Pharmaceutical Companies of Johnson & Johnson
Co-moderator


Dominic Clarke
VP of Technical Operations, IntegriCell
Cryoport, Inc.
Co-moderator


Tracey Hlucky
Senior Manager, Regional Quality Operations- US
Kite Pharma (a Gilead Company)
Panelist


Kathy Loper
Director, Regulatory Affairs
NMDP BioTherapies
Panelist


Joseph Schwartz
Director, Transfusion Services
Moffitt Cancer Center
Panelist